Monday, 14 May 2012

Dermacort Hydrocortisone Cream (Marlborough Pharmaceuticals Ltd)





1. Name Of The Medicinal Product



Dermacort Hydrocortisone Cream


2. Qualitative And Quantitative Composition



Dermacort Hydrocortisone Cream contains hydrocortisone B.P. 0.1% w/w in a specially formulated, lanolin-free cream base.



3. Pharmaceutical Form



Cream.



4. Clinical Particulars



4.1 Therapeutic Indications



Topical treatment of skin irritations, contact dermatitis, allergic contact dermatitis and rashes due to reactions to plants, insect bite, jewellery, toiletries, deodorants, soaps and detergents. Dermacort is also indicated for the treatment of mild to moderate eczema.



4.2 Posology And Method Of Administration



For cutaneous use.



Adults and children over 10 years:



Apply a thin layer to cover the affected area once or twice a day.



Rub in gently until the cream disappears.



Do not use for more than one week.



4.3 Contraindications



For external use only.



Known sensitivity to hydrocortisone and/or other excipients in this product.



Do not use on the eyes or face, the ano-genital region, on broken or infected skin.



As with all topical steroids, Dermacort is contra-indicated in the presence of viral, bacterial and fungal diseases of the skin.



4.4 Special Warnings And Precautions For Use



See above



4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction



None known



4.6 Pregnancy And Lactation



There is inadequate evidence of safety in human pregnancy. Topical administration of corticosteroids to pregnant animals can cause abnormalities of foetal development including cleft palate and intrauterine growth retardation.



Dermacort should not be used during pregnancy.



4.7 Effects On Ability To Drive And Use Machines



Not applicable.



4.8 Undesirable Effects



Dermacort is normally well tolerated, but if signs of hypersensitivity appear application should stop immediately.



4.9 Overdose



Acute overdosage is very unlikely to occur, however, in the case of chronic overdosage or misuse, the features of hypercorticism may appear and in this situation topical steroids should be discontinued.



5. Pharmacological Properties



5.1 Pharmacodynamic Properties



Corticosteroids are used in pharmacological doses for their anti-inflammatory and immunosuppressive glucocorticoid properties which suppress the clinical manifestation of a wide range of disease. Although many synthetic derivatives have been developed, hydrocortisone is still used widely in topical formulations for mild and transient inflammatory dermatitis. It has the advantage over its synthetic derivatives that it is metabolised in the skin and therefore cannot accumulate to form a depot, which may result in local side effects.



5.2 Pharmacokinetic Properties



The cream formulation of Dermacort was developed in order to optimise the release and partition of its active ingredient, hydrocortisone, into the skin. The hydrocortisone is presented as a saturated or near saturated solution in aqueous propylene glycol, which represents the continuous phase of the emulsion system. It has been shown, by the vasoconstrictor assay on normal skin, that in this environment, a 0.1% concentration of the hydrocortisone is equivalent to the 1% concentration where the drug substance is in suspension. Clinical studies have confirmed that 0.1% Dermacort is equivalent to 1.0% hydrocortisone cream BP/BPC whilst the reduced strength of Dermacort increases the margin of safety.



5.3 Preclinical Safety Data



None applicable.



6. Pharmaceutical Particulars



6.1 List Of Excipients



Propylene Glycol



Emulsifying Ointment



Citric Acid



Purified Water



6.2 Incompatibilities



None stated.



6.3 Shelf Life



24 months.



6.4 Special Precautions For Storage



None.



6.5 Nature And Contents Of Container



Lacquered Aluminium Tubes containing 15 g of cream



6.6 Special Precautions For Disposal And Other Handling



None.



7. Marketing Authorisation Holder



Marlborough Pharmaceuticals Ltd, 35A High Street, Marlborough, Wilts SN8 1LW



8. Marketing Authorisation Number(S)



PL 23138/0007



9. Date Of First Authorisation/Renewal Of The Authorisation



01/03/2007



10. Date Of Revision Of The Text




Saturday, 12 May 2012

Seroquel XR



Generic Name: quetiapine (Oral route)


kwe-TYE-a-peen FUE-ma-rate


Oral route(Tablet;Tablet, Extended Release)

Elderly patients with dementia-related psychosis treated with atypical antipsychotic drugs are at an increased risk of death compared to placebo. Although the causes of death were varied in clinical trials, most of the deaths appeared to be either cardiovascular (e.g., heart failure, sudden death) or infectious (e.g., pneumonia) in nature. Not approved for the treatment of patients with dementia-related psychosis. Antidepressants increased the risk of suicidal thinking and behavior in children, adolescents, and young adults in short-term studies with major depressive disorder (MDD) and other psychiatric disorders. Short term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24, and there was a reduction in risk with antidepressants compared to placebo in adults aged 65 and older. This risk must be balanced with the clinical need. Monitor patients closely for clinical worsening, suicidality, or unusual changes in behavior. Families and caregivers should be advised of the need for close observation and communication with the prescriber. Regular strength tablets not approved for use in patients under 10 years of age ; extended-release tablets not approved for use in patients under 18 years of age .



Commonly used brand name(s)

In the U.S.


  • Seroquel

  • Seroquel XR

Available Dosage Forms:


  • Tablet

  • Tablet, Extended Release

Therapeutic Class: Antipsychotic


Chemical Class: Quetiapine


Uses For Seroquel XR


Quetiapine is used to treat nervous, emotional, and mental conditions (e.g., schizophrenia). It may be used alone or together with other medicines (e.g., lithium or divalproex) to treat symptoms of bipolar disorder (manic-depressive illness) or mania that is part of bipolar disorder. This medicine should not be used to treat behavioral problems in older adult patients who have dementia or Alzheimer's disease.


Quetiapine extended-release tablets is also used together with other medicines to treat major depressive disorder (MDD) in adults.


This medicine is available only with your doctor's prescription.


Before Using Seroquel XR


In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.


Pediatric


Appropriate studies have not been performed on the relationship of age to the effects of quetiapine tablets in children with schizophrenia younger than 13 years of age, in children with bipolar mania younger than 10 years of age, and in children with bipolar depression younger than 18 years of age. Safety and efficacy have not been established in these age groups.


Appropriate studies have not been performed on the relationship of age to the effects of quetiapine extended-release tablets in the pediatric population. Safety and efficacy have not been established.


Geriatric


Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of quetiapine in the elderly. However, elderly patients are more likely to have dementia or age-related heart, liver, or kidney problems, which may require caution and an adjustment in the dose for patients receiving quetiapine.


Pregnancy








Pregnancy CategoryExplanation
All TrimestersCAnimal studies have shown an adverse effect and there are no adequate studies in pregnant women OR no animal studies have been conducted and there are no adequate studies in pregnant women.

Breast Feeding


There are no adequate studies in women for determining infant risk when using this medication during breastfeeding. Weigh the potential benefits against the potential risks before taking this medication while breastfeeding.


Interactions with Medicines


Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are taking this medicine, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.


Using this medicine with any of the following medicines is not recommended. Your doctor may decide not to treat you with this medication or change some of the other medicines you take.


  • Bepridil

  • Cisapride

  • Dronedarone

  • Fluconazole

  • Mesoridazine

  • Metoclopramide

  • Pimozide

  • Posaconazole

  • Terfenadine

  • Thioridazine

Using this medicine with any of the following medicines is usually not recommended, but may be required in some cases. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Acecainide

  • Ajmaline

  • Alfuzosin

  • Amiodarone

  • Amitriptyline

  • Amobarbital

  • Amoxapine

  • Apomorphine

  • Aprindine

  • Aprobarbital

  • Arsenic Trioxide

  • Asenapine

  • Astemizole

  • Azimilide

  • Azithromycin

  • Betamethasone

  • Bretylium

  • Butabarbital

  • Butalbital

  • Chloral Hydrate

  • Chloroquine

  • Chlorpromazine

  • Ciprofloxacin

  • Citalopram

  • Clarithromycin

  • Clomipramine

  • Clozapine

  • Cortisone

  • Crizotinib

  • Dasatinib

  • Deflazacort

  • Desipramine

  • Dexamethasone

  • Dibenzepin

  • Disopyramide

  • Dofetilide

  • Dolasetron

  • Doxepin

  • Droperidol

  • Encainide

  • Enflurane

  • Erythromycin

  • Eterobarb

  • Flecainide

  • Fluoxetine

  • Foscarnet

  • Gatifloxacin

  • Gemifloxacin

  • Granisetron

  • Halofantrine

  • Haloperidol

  • Halothane

  • Hydrocortisone

  • Hydromorphone

  • Hydroquinidine

  • Ibutilide

  • Iloperidone

  • Imipramine

  • Isoflurane

  • Isradipine

  • Lapatinib

  • Levofloxacin

  • Lidoflazine

  • Lorcainide

  • Lumefantrine

  • Mefloquine

  • Mephobarbital

  • Methadone

  • Methohexital

  • Methylprednisolone

  • Milnacipran

  • Moxifloxacin

  • Nilotinib

  • Norfloxacin

  • Nortriptyline

  • Octreotide

  • Ofloxacin

  • Ondansetron

  • Paliperidone

  • Paramethasone

  • Pazopanib

  • Pentamidine

  • Pentobarbital

  • Perflutren Lipid Microsphere

  • Phenobarbital

  • Pirmenol

  • Prajmaline

  • Prednisolone

  • Prednisone

  • Primidone

  • Probucol

  • Procainamide

  • Prochlorperazine

  • Promethazine

  • Propafenone

  • Protriptyline

  • Quinidine

  • Quinine

  • Ranolazine

  • Rifampin

  • Risperidone

  • Salmeterol

  • Secobarbital

  • Sematilide

  • Sodium Phosphate

  • Sodium Phosphate, Dibasic

  • Sodium Phosphate, Monobasic

  • Solifenacin

  • Sorafenib

  • Sotalol

  • Sparfloxacin

  • Spiramycin

  • Sulfamethoxazole

  • Sunitinib

  • Tedisamil

  • Telavancin

  • Telithromycin

  • Tetrabenazine

  • Thiopental

  • Toremifene

  • Trazodone

  • Triamcinolone

  • Trifluoperazine

  • Trimethoprim

  • Trimipramine

  • Vandetanib

  • Vardenafil

  • Vasopressin

  • Vemurafenib

  • Voriconazole

  • Ziprasidone

  • Zolmitriptan

Using this medicine with any of the following medicines may cause an increased risk of certain side effects, but using both drugs may be the best treatment for you. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Fosphenytoin

  • Ketoconazole

  • Phenytoin

  • Warfarin

Interactions with Food/Tobacco/Alcohol


Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.


Using this medicine with any of the following may cause an increased risk of certain side effects but may be unavoidable in some cases. If used together, your doctor may change the dose or how often you use this medicine, or give you special instructions about the use of food, alcohol, or tobacco.


  • Ethanol

Other Medical Problems


The presence of other medical problems may affect the use of this medicine. Make sure you tell your doctor if you have any other medical problems, especially:


  • Blood vessel or circulation problems or

  • Dehydration or

  • Heart attack or stroke, history of or

  • Heart disease (e.g., heart hypertrophy) or

  • Heart failure or

  • Heart rhythm problems (e.g., QT prolongation), or

  • Hypotension (low blood pressure) or

  • Hypovolemia (low blood volume)—May cause side effects to become worse.

  • Bradycardia (slow heartbeat), history of or

  • Heart rhythm problem (e.g., congenital long QT interval) or

  • Hypokalemia (low potassium in the blood) or

  • Hypomagnesemia (low magnesium in the blood)—May increase risk for more serious side effects.

  • Breast cancer, prolactin dependent or

  • Cataracts or

  • Hyperlipidemia (high blood cholesterol or fats) or

  • Hyperprolactinemia (high prolactin in the blood) or

  • Hypertension (high blood pressure) or

  • Hypothyroidism (underactive thyroid) or

  • Liver disease or

  • Seizures, history of or

  • Trouble with swallowing—Use with caution. May make these conditions worse.

  • Diabetes or

  • Hyperglycemia—This medicine may raise your blood sugar levels.

Proper Use of quetiapine

This section provides information on the proper use of a number of products that contain quetiapine. It may not be specific to Seroquel XR. Please read with care.


Take this medicine exactly as directed by your doctor to benefit your condition as much as possible. Do not take more of it, do not take it more often, and do not take it for a longer time than your doctor ordered.


This medicine should come with a Medication Guide. It is very important that you read and understand this information. Be sure to ask your doctor about anything you do not understand.


Quetiapine tablets may be taken with or without food on a full or empty stomach. However, if your doctor tells you to take it a certain way, take it as directed.


Swallow the extended-release tablets whole. Do not break, crush, or chew it. It is best to take this medicine without food or with a light meal (approximately 300 calories).


Dosing


The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.


The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.


  • For oral dosage form (extended-release tablets):
    • For treatment of depression with bipolar disorder:
      • Adults—At first, 50 milligrams (mg) once per day in the evening. Your doctor may adjust your dose as needed. However, the dose is usually not more than 300 mg per day.

      • Children—Use and dose must be determined by the doctor.


    • For treatment of mania with bipolar disorder:
      • Adults—At first, 300 milligrams (mg) once per day in the evening. Your doctor may adjust your dose as needed. However, the dose is usually not more than 800 mg per day.

      • Children—Use and dose must be determined by the doctor.


    • For treatment of major depressive disorder (MDD):
      • Adults—At first, 50 milligrams (mg) once per day in the evening. Your doctor may adjust your dose as needed. However, the dose is usually not more than 300 mg per day.

      • Children—Use and dose must be determined by the doctor.


    • For treatment of schizophrenia:
      • Adults—At first, 300 milligrams (mg) once per day in the evening. Your doctor may adjust your dose as needed. However, the dose is usually not more than 800 mg per day.

      • Children—Use and dose must be determined by the doctor.



  • For oral dosage form (tablets):
    • For treatment of depression with bipolar disorder:
      • Adults—At first, 50 milligrams (mg) once per day at bedtime. The dose is usually increased daily to reach 300 mg per day on the fourth day. Your doctor may adjust your dose as needed. However, the dose is usually not more than 600 mg per day.

      • Children—Use and dose must be determined by the doctor. .


    • For treatment of mania with bipolar disorder:
      • Adults—At first, 100 milligrams (mg) per day, given in two equally divided doses. The dose is usually increased to 400 mg per day, which is divided and given in two doses per day. Your doctor may adjust your dose as needed. However, the dose is usually not more than 800 mg per day.

      • Children 10 to 17 years of age—At first, 25 milligrams (mg) two times per day. Your doctor may adjust your dose as needed. However, the dose is usually not more than 600 mg per day.

      • Children younger than 10 years of age—Use and dose must be determined by the doctor.


    • For treatment of schizophrenia:
      • Adults—At first, 25 milligrams (mg) two times per day. The dose is usually increased to 300 to 400 mg per day, which is divided and given in two or three doses per day. Your doctor may adjust your dose as needed. However, the dose is usually not more than 800 mg per day.

      • Teenagers 13 to 17 years of age—At first, 25 milligrams (mg) two times per day. Your doctor may adjust your dose as needed. However, the dose is usually not more than 800 mg per day.

      • Children younger than 13 years of age—Use and dose must be determined by the doctor.



Missed Dose


If you miss a dose of this medicine, take it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses.


Storage


Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


Ask your healthcare professional how you should dispose of any medicine you do not use.


Precautions While Using Seroquel XR


It is very important that your doctor should check the progress of you or your child at regular visits to make sure this medicine is working properly. Blood tests may be needed to check for unwanted effects. You may also need to have your or your child's eyes tested on a regular basis.


This medicine may add to the effects of alcohol and other CNS depressants (medicines that make you drowsy or less alert). Some examples of CNS depressants are antihistamines or medicine for hay fever, other allergies, or colds; sedatives, tranquilizers, or sleeping medicine; prescription pain medicine or narcotics; medicine for seizures or barbiturates; muscle relaxants; or anesthetics, including some dental anesthetics. Check with your doctor before taking any of the above while you or your child are using quetiapine.


For some patients, this medicine can increase thoughts of suicide. Tell your doctor right away if you or your child start to feel more depressed and have thoughts about hurting yourself. Report any unusual thoughts or behaviors that trouble you, especially if they are new or are getting worse quickly. Make sure the doctor knows if you or your child have trouble sleeping, get upset easily, have a big increase in energy, or start to act reckless. Also tell the doctor if you have sudden or strong feelings, such as feeling nervous, angry, restless, violent, or scared. Let the doctor know if you or anyone in your family has bipolar disorder (manic-depressive illness) or has tried to commit suicide.


Quetiapine may cause drowsiness, trouble with thinking, or trouble with your vision (especially during the first week of use). Make sure you know how you react to this medicine before you drive, use machines, or do other jobs that require you to be alert, well-coordinated, or able to think or see well.


This medicine may increase the amount of sugar in your blood. Check with your doctor right away if you have increased thirst or urination. If you or your child have diabetes, you may notice a change in the results of your urine or blood sugar tests. Check your blood sugar closely and talk with your doctor if you have any questions.


Check with your doctor right away if you or your child are having convulsions (seizures); difficulty with breathing; a fast heartbeat; high fever; high or low blood pressure; increased sweating; loss of bladder control; severe muscle stiffness; unusually pale skin; or tiredness. These could be symptoms of a serious condition called neuroleptic malignant syndrome (NMS).


Dizziness, lightheadedness, or fainting may occur, especially when you get up from a lying or sitting position. Getting up slowly may help. If the problem continues or gets worse, check with your doctor.


Quetiapine can temporarily lower the number of white blood cells in your blood, increasing the chance of getting an infection. It can also lower the number of platelets, which are necessary for proper blood clotting. If this occurs, there are certain precautions you can take, especially when your blood count is low, to reduce the risk of infection or bleeding:


  • If you can, avoid people with infections. Check with your doctor immediately if you or your child think you are getting an infection or if you get a fever or chills, cough or hoarseness, lower back or side pain, or painful or difficult urination.

  • Check with your doctor immediately if you or your child notice any unusual bleeding or bruising; black, tarry stools; blood in the urine or stools; or pinpoint red spots on your skin.

  • Be careful when using a regular toothbrush, dental floss, or toothpick. Your medical doctor, dentist, or nurse may recommend other ways to clean your teeth and gums. Check with your medical doctor before having any dental work done.

  • Do not touch your eyes or the inside of your nose unless you have just washed your hands and have not touched anything else in the meantime.

  • Be careful not to cut yourself when you are using sharp objects such as a safety razor or fingernail or toenail cutters.

  • Avoid contact sports or other situations where bruising or injury could occur.

This medicine may cause tardive dyskinesia (a movement disorder). Check with your doctor right away if you or your child have any of the following symptoms while taking this medicine: lip smacking or puckering, puffing of the cheeks, rapid or worm-like movements of the tongue, uncontrolled chewing movements, or uncontrolled movements of the arms and legs.


Quetiapine may increase your cholesterol and fats in the blood. If this condition occurs, your doctor may give you or your child some medicines that can lower the amount of cholesterol and fats in the blood.


This medicine may increase your weight. Your doctor may need to check your or your child's weight on a regular basis while you are using this medicine.


You will need to have your blood pressure measured before starting this medicine and while you or your child are using it. If you notice any change to your recommended blood pressure, call your doctor right away. If you have questions about this, talk to your doctor.


This medicine can cause changes in heart rhythms, such as a condition called QT prolongation. It may change the way your heart beats and cause fainting or serious side effects in some patients. Contact your doctor right away if you or your child have any symptoms of heart rhythm problems, such as fast, pounding, or uneven heartbeats.


Quetiapine may make it more difficult for your body to cool down. It might reduce how much you sweat. Your body could get too hot if you do not sweat enough. If your body gets too hot, you might feel dizzy, weak, tired, or confused. You might vomit or have an upset stomach. Do not get too hot while you are exercising. Avoid places that are very hot. Call your doctor if you or your child are too hot and can not cool down.


Do not suddenly stop taking your this medicine without checking first with your doctor. Your doctor may want you or your child to gradually reduce the amount you are using before stopping it completely. This is to decrease the chance of having symptoms such as nausea, sleeplessness, trouble in sleeping, unable to sleep, or vomiting.


Before you have any medical tests, tell the medical doctor in charge that you are taking this medicine. The results of some tests (e.g., urine drug screens) may be affected by this medicine.


Do not take other medicines unless they have been discussed with your doctor. This includes prescription or nonprescription (over-the-counter [OTC]) medicines and herbal or vitamin supplements.


Seroquel XR Side Effects


Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.


Check with your doctor immediately if any of the following side effects occur:


More common
  • Chills

  • cold sweats

  • confusion

  • dizziness, faintness, or lightheadedness when getting up suddenly from a lying or sitting position

  • sleepiness or unusual drowsiness

Less common
  • Black, tarry stools

  • blurred vision

  • changes in patterns and rhythms of speech

  • chest pain

  • cough

  • difficulty with swallowing

  • drooling

  • fever, muscle aches, or sore throat

  • inability to move the eyes

  • inability to sit still

  • increased blinking or spasms of the eyelid

  • lip smacking or puckering

  • loss of balance control

  • mask-like face

  • need to keep moving

  • painful or difficult urination

  • puffing of the cheeks

  • rapid or worm-like movements of the tongue

  • restlessness

  • shakiness in the legs, arms, hands, or feet

  • shortness of breath

  • shuffling walk

  • slowed movements

  • slurred speech

  • sores, ulcers, or white spots on the lips or in the mouth

  • sticking out of the tongue

  • stiffness of the arms or legs

  • sweating

  • swelling of the face, arms, hands, feet, or lower legs

  • swollen glands

  • trembling and shaking of the hands and fingers

  • trouble with breathing, speaking, or swallowing

  • uncontrolled chewing movements

  • uncontrolled movements of the arms and legs

  • uncontrolled twisting movements of the neck, trunk, arms, or legs

  • unusual bleeding or bruising

  • unusual facial expressions

  • unusual tiredness or weakness

Rare
  • Dry, puffy skin

  • fast, pounding, or irregular heartbeat

  • loss of appetite

  • menstrual changes

  • tiredness

  • unusual secretion of milk (in females)

  • weight gain

Incidence not known
  • Aching or discomfort in the lower legs or sensation of crawling in the legs

  • hives

  • itching

  • painful or prolonged erection of the penis

  • puffiness or swelling of the eyelids or around the eyes, face, lips, or tongue

  • skin rash

  • tightness in the chest

  • tingling of the hands or feet

  • unusual weight gain or loss

  • wheezing

Get emergency help immediately if any of the following symptoms of overdose occur:


Symptoms of overdose
  • Convulsions (seizures)

  • decreased urine

  • dry mouth

  • increased thirst

  • low blood pressure

  • mood changes

  • muscle pain or cramps

  • nausea or vomiting

  • numbness or tingling in the hands, feet, or lips

  • weakness

Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:


More common
  • Constipation

  • headache

Less common
  • Abnormal vision

  • acid or sour stomach

  • belching

  • decreased appetite

  • decreased strength and energy

  • headache

  • heartburn

  • increased appetite

  • increased muscle tone

  • increased sweating

  • increased weight

  • indigestion

  • sneezing

  • stomach discomfort, upset, or pain

  • stuffy or runny nose

Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.

See also: Seroquel XR side effects (in more detail)



The information contained in the Thomson Reuters Micromedex products as delivered by Drugs.com is intended as an educational aid only. It is not intended as medical advice for individual conditions or treatment. It is not a substitute for a medical exam, nor does it replace the need for services provided by medical professionals. Talk to your doctor, nurse or pharmacist before taking any prescription or over the counter drugs (including any herbal medicines or supplements) or following any treatment or regimen. Only your doctor, nurse, or pharmacist can provide you with advice on what is safe and effective for you.


The use of the Thomson Reuters Healthcare products is at your sole risk. These products are provided "AS IS" and "as available" for use, without warranties of any kind, either express or implied. Thomson Reuters Healthcare and Drugs.com make no representation or warranty as to the accuracy, reliability, timeliness, usefulness or completeness of any of the information contained in the products. Additionally, THOMSON REUTERS HEALTHCARE MAKES NO REPRESENTATION OR WARRANTIES AS TO THE OPINIONS OR OTHER SERVICE OR DATA YOU MAY ACCESS, DOWNLOAD OR USE AS A RESULT OF USE OF THE THOMSON REUTERS HEALTHCARE PRODUCTS. ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE OR USE ARE HEREBY EXCLUDED. Thomson Reuters Healthcare does not assume any responsibility or risk for your use of the Thomson Reuters Healthcare products.


More Seroquel XR resources


  • Seroquel XR Side Effects (in more detail)
  • Seroquel XR Use in Pregnancy & Breastfeeding
  • Seroquel XR Drug Interactions
  • Seroquel XR Support Group
  • 59 Reviews for Seroquel XR - Add your own review/rating


  • Seroquel XR Prescribing Information (FDA)

  • Seroquel XR Sustained-Release Tablets MedFacts Consumer Leaflet (Wolters Kluwer)

  • Quetiapine MedFacts Consumer Leaflet (Wolters Kluwer)

  • Quetiapine Fumarate Monograph (AHFS DI)

  • Seroquel Consumer Overview

  • Seroquel Prescribing Information (FDA)



Compare Seroquel XR with other medications


  • Bipolar Disorder
  • Borderline Personality Disorder
  • Depression
  • Generalized Anxiety Disorder
  • Insomnia
  • Obsessive Compulsive Disorder
  • Paranoid Disorder
  • Post Traumatic Stress Disorder
  • Schizoaffective Disorder
  • Schizophrenia
  • Tourette's Syndrome

Tuesday, 8 May 2012

Boots Effervescent Health Salts





Boots Effervescent Health Salts


(Magnesium Sulphate, Sodium Bicarbonate, Citric acid)



Sparkling relief of upset stomach, heartburn, indigestion and occasional constipation


227 g



Read all of this label for full instructions.



Uses: An antacid and laxative for the relief of upset stomach, heartburn, indigestion, feeling sick and for the relief of occasional constipation.





Before you take this medicine



Do not take:



  • If you are allergic to any of the ingredients


  • If you have severe stomach problems


  • If you have an intolerance to some sugars, unless your doctor tells you to (this medicine contains sucrose)



Talk to your pharmacist or doctor:


  • If you have heart, kidney or liver problems

  • If you have diabetes

  • If you need to use a laxative every day

  • If you have severe stomach pain

  • If you are elderly, or feel very weak

  • If you are on a controlled sodium diet (each level teaspoon of powder contains 185 mg sodium)

  • If you are pregnant or breastfeeding




How to take this medicine


Check the inner seal is not broken before first use. If it is, do not use the powder.


Use a dry spoon to measure. Mix the amount in the table with a glass of water and drink the solution, before it stops fizzing. Replace lid firmly after use.



Adults:



For upset stomach, heartburn, indigestion, feeling sick: One or two teaspoonfuls.



For constipation: Two teaspoonfuls before breakfast or at bedtime.



Children of 3 years and over: Reduce the amount above according to size and age.



Do not give to children under 3 years.


Do not take this medicine for long periods of time (generally more than a week).


Do not take more than the amount recommended.


If symptoms worsen talk to your doctor. If symptoms don’t go away talk to your doctor.




Possible side effects


Most people will not have problems, but some may get some of these:


  • Gripping pain in your stomach

  • Diarrhoea, feeling sick, being sick

If you have taken the medicine for a long time you may get:


  • Light headedness, confusion

  • Muscle weakness, cramps

  • Numbness, tingling, breathing problems


If any side effect becomes severe, or you notice any side effect not listed here, please tell your pharmacist or doctor.



Store in a dry place below 25°C and away from strong smells.



Keep all medicines out of the sight and reach of children.


Use by the date on the base of the tub. Throw away any powder left 3 months after opening.



Active ingredients: This effervescent powder contains Citric Acid 19.5% w/w, Magnesium Sulphate 17.4% w/w, Sodium Bicarbonate 22.6% w/w.


Also contains: sucrose.


PL12063/0039


Text prepared 4/08


Manufactured for



The Boots Company PLC

Nottingham

NG2 3AA


by the MA holder



Wrafton Laboratories Limited

Braunton

Devon

EX33 2DL


If you need more advice ask your pharmacist.





Monday, 7 May 2012

Potassium Phosphate


Pronunciation: poe-TAS-ee-um FOS-fate
Generic Name: Potassium Phosphate
Brand Name: K-Phos Original


Potassium Phosphate is used for:

Preventing kidney stones. It is also used to increase the effectiveness of certain antibacterial medicines (methenamine mandelate and methenamine hippurate). It may also be used for other conditions as determined by your doctor.


Potassium Phosphate is a urinary acidifier. It works by increasing the amount of acid in the urine, which lowers the pH of the urine. This may reduce the growth of some bacteria in the urine and help dissolve calcium kidney stones.


Do NOT use Potassium Phosphate if:


  • you are allergic to any ingredient in Potassium Phosphate

  • you have infected kidney stones or severe kidney problems

  • you have decreased urination or are unable to urinate

  • you have high levels of phosphate or potassium in the blood

Contact your doctor or health care provider right away if any of these apply to you.



Before using Potassium Phosphate:


Some medical conditions may interact with Potassium Phosphate. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


  • if you are pregnant, planning to become pregnant, or are breast-feeding

  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

  • if you have allergies to medicines, foods, or other substances

  • if you have low blood calcium levels or you are on a potassium-restricted diet

  • if you have a history of heart problems (eg, heart failure), kidney problems, kidney or other urinary stones, certain muscle problems (eg, myotonia congenita, rhabdomyolysis), stomach or bowel problems (eg, inflammation), liver problems, adrenal gland problems (eg, Addison disease), inflammation of the pancreas, or parathyroid problems

  • if you are dehydrated or have rickets, softened or weakened bones, or a urinary tract infection

  • if you have a condition in which your skin is breaking down (eg, severe burns)

Some MEDICINES MAY INTERACT with Potassium Phosphate. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • Aldosterone blockers (eg, eplerenone), aliskiren, angiotensin-converting enzyme (ACE) inhibitors (eg, enalapril), potassium-sparing diuretics (eg, triamterene), or potassium supplements because the risk of high potassium levels, possibly with irregular heartbeat or a heart attack, may be increased

  • Digoxin or salicylates (eg, aspirin) because the risk of their side effects may be increased by Potassium Phosphate

This may not be a complete list of all interactions that may occur. Ask your health care provider if Potassium Phosphate may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.


How to use Potassium Phosphate:


Use Potassium Phosphate as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Potassium Phosphate is usually taken with meals and at bedtime. Ask your doctor when you should take Potassium Phosphate.

  • Do not swallow Potassium Phosphate whole. Dissolve 2 tablets in 6 to 8 oz (180 to 240 mL) of water. Allow the tablets to dissolve for 2 to 5 minutes or more, if necessary. Stir to be sure the medicine is completely dissolved. If any tablet particles do not dissolve, crush them and stir well.

  • If your doctor has told you to use a different dose, ask your pharmacist how much water to use to dissolve the medicine.

  • Do not take antacids that have aluminum, magnesium, or calcium with Potassium Phosphate without checking with your doctor or pharmacist.

  • If you miss a dose of Potassium Phosphate, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Potassium Phosphate.



Important safety information:


  • Potassium Phosphate may cause dizziness. This effect may be worse if you take it with alcohol or certain medicines. Use Potassium Phosphate with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

  • While taking Potassium Phosphate, the possibility of passing old kidney stones is increased.

  • Check with your doctor before you use a salt substitute or a product that has potassium in it.

  • Lab tests, including kidney function and electrolyte levels (eg, calcium, potassium, phosphorus), may be performed while you use Potassium Phosphate. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

  • PREGNANCY and BREAST-FEEDING: It is not known if Potassium Phosphate can cause harm to the fetus. If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Potassium Phosphate while you are pregnant. It is not known if Potassium Phosphate is found in breast milk. If you are or will be breast-feeding while you use Potassium Phosphate, check with your doctor. Discuss any possible risks to your baby.


Possible side effects of Potassium Phosphate:


All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:



Diarrhea; nausea; stomach pain; vomiting.



Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bone or joint pain; confusion; decreased urination; dizziness; irregular heartbeat; muscle cramps; numbness, tingling, pain, or weakness in the hands or feet; numbness or tingling around the lips; seizures; severe or persistent diarrhea; shortness of breath; unusual tiredness; unusual weakness or heaviness of the legs.



This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.



If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.


Proper storage of Potassium Phosphate:

Store Potassium Phosphate at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Potassium Phosphate out of the reach of children and away from pets.


General information:


  • If you have any questions about Potassium Phosphate, please talk with your doctor, pharmacist, or other health care provider.

  • Potassium Phosphate is to be used only by the patient for whom it is prescribed. Do not share it with other people.

  • If your symptoms do not improve or if they become worse, check with your doctor.

  • Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Potassium Phosphate. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

Saturday, 5 May 2012

Elleste Solo 1mg & 2mg







Elleste Solo 1 mg and 2 mg




(estradiol hemihydrate)



Read all of this leaflet carefully before you start using this medicine.


  • Keep this leaflet. You may need to read it again.

  • If you have any further questions, please ask your doctor or pharmacist.

  • This medicine has been prescribed for you. Do not pass it on to others. It may harm them, even if their symptoms are the same as yours.

  • If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.



In this leaflet:


  • 1. What Elleste Solo is and what it is used for

  • 2. Before you take Elleste Solo

  • 3. How to take Elleste Solo

  • 4. Possible side effects

  • 5. How to store Elleste Solo

  • 6. Further information




What Elleste Solo Is And What It Is Used For


Elleste Solo is a form of hormone replacement therapy (HRT).


It contains the hormone estradiol hemihydrate, and is one of a group of medicines called estrogen-only preparations. It is not an oral contraceptive.



Why has your doctor given you Elleste Solo?


Elleste Solo treats the symptoms of the menopause (change of life). It is usually given to women who have had a hysterectomy (had their womb removed).


As you approach the menopause, your ovaries gradually produce fewer hormones. This may cause unpleasant symptoms such as hot flushes and sweating. Elleste Solo replaces a hormone which you lose during the menopause and prevents or relieves any unpleasant symptoms.


You doctor will aim to give you the lowest dose required to treat your symptoms.


Other changes in your bones may also take place over a longer time. These changes can lead to an increased risk of your bones breaking or cracking. If you are at an increased risk of fractures due to osteoporosis (thinning of the bones) but are unable to take other treatments or if other therapies prove to be ineffective, Elleste Solo 2 mg may also be used for this purpose. Your doctor should discuss all the available options with you.





Before You Take Elleste Solo


Elleste Solo may not be suitable for all women.


Read the list below.




DO NOT take Elleste Solo, if you have, or have ever had:


  • a blood clot in a vein in your leg or anywhere else (a "deep vein thrombosis");

  • a blood clot that has travelled to your lung or another part of the body (an "embolus");

  • narrowed or blocked arteries possibly leading to angina and heart disease;

  • breast or womb cancer;

  • unexplained vaginal bleeding;

  • liver problems, for example, jaundice (yellowing of the skin or eyes);

  • porphyria (a rare inherited blood disease);

  • untreated endometrial hyperplasia (an overgrowth of the lining of your womb).

Also do not take Elleste Solo if you:


  • are pregnant or think you could be pregnant;

  • are breast-feeding;

  • have ever had an allergic reaction to any of the ingredients in Elleste Solo (see Section 6).

Elleste Solo contains lactose. If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.



Sunset yellow colouring in Elleste Solo 2mg can cause allergic-type reactions, including asthma. This allergy is more common in people who are allergic to aspirin.




Safety of HRT



As well as benefits, HRT has some risks which you need to consider when you're deciding whether to take it, or whether to carry on taking it.





Take special care with Elleste Solo Tablets


Elleste Solo might have an effect on various processes in your body. HRT should only be started for symptoms that reduce your quality of life.





Medical check-ups



Before you start taking HRT, your doctor should ask about your own and your family's medical history. Your doctor may decide to examine your breasts and/or your abdomen, and may do an internal examination - but only if these examinations are necessary for you, or if you have any special concerns.



Once you've started on HRT, you should:


  • see your doctor for regular check-ups (at least once a year). At these check-ups, your doctor may discuss with you the benefits and risks of continuing to take HRT;


  • go for regular breast screening and cervical smear tests;


  • regularly check your breasts for any changes such as dimpling of the skin, changes in the nipple, or any lumps you can see or feel.




Effects on your heart or circulation



Heart disease:



HRT is not recommended for women who have heart disease, now or in the past. If you have ever had heart disease, talk to your doctor to see if you should be taking HRT.


HRT will not help to prevent heart disease.


Studies with one type of HRT (containing conjugated estrogen plus the progestogen MPA) have shown that women may be slightly more likely to get heart disease during the first year of taking the medication. For other types of HRT, the risk is likely to be similar, although this is not yet certain.




If you get:


  • a pain in your chest that spreads to your arm or neck


See a doctor as soon as possible and do not take any more HRT until your doctor says you can. This pain could be a sign of heart disease.



Stroke:


Recent research suggests that HRT slightly increases the risk of having a stroke. Other factors that can increase the risk of stroke include:


  • getting older

  • high blood pressure

  • smoking

  • drinking too much alcohol

  • an irregular heartbeat.


If you are worried about any of these things, or if you have had a stroke in the past, talk to your doctor to see if you should take HRT.




Compare


Looking at women in their 50s who are not taking HRT - on average, over a 5-year period, 3 in 1000 would be expected to have a stroke.


For women in their 50s who are taking HRT, the figure would be 4 in 1000.


Looking at women in their 60s who are not taking HRT - on average, over a 5-year period, 11 in 1000 would be expected to have a stroke.


For women in their 60s who are taking HRT, the figure would be 15 in 1000.




If you get:


  • unexplained migraine-type headaches, with or without disturbed vision


See a doctor as soon as possible and do not take any more HRT until your doctor says you can. These headaches may be an early warning sign of a stroke.



Blood clots:


HRT may increase the risk of blood clots in the veins (also called deep vein thrombosis, or DVT), especially during the first year of taking it.


These blood clots are not always serious, but if one travels to the lungs, it can cause chest pain, breathlessness, collapse or even death. This condition is called pulmonary embolism, or PE.


DVT and PE are examples of a condition called venous thromboembolism, or VTE.



You are more likely to get a blood clot if you:


  • are seriously overweight

  • have had a blood clot before or have a close family member who has had blood clots

  • have had one or more miscarriages

  • have any blood clotting problem that needs treatment with a medicine such as warfarin

  • are off your feet for a long time because of major surgery, injury or illness

  • have a rare condition called systemic lupus erythematosus (SLE).


If any of these apply to you, talk to your doctor to see if you should take HRT.




Compare


Looking at women in their 50s who are not taking HRT - on average, over a 5-year period, 3 in 1000 would be expected to get a blood clot.


For women in their 50s who are taking HRT, the figure would be 7 in 1000.


Looking at women in their 60s who are not taking HRT - on average, over a 5-year period, 8 in 1000 would be expected to get a blood clot.


For women in their 60s who are taking HRT, the figure would be 17 in 1000.




The following may be signs of blood clot if you get:


  • painful swelling in your leg

  • sudden chest pain

  • difficulty breathing


See a doctor as soon as possible and do not take any more HRT until your doctor says you can.



If you're going to have surgery, make sure your doctor knows about it. You may need to stop taking HRT about 4 to 6 weeks before the operation, to reduce the risk of a blood clot.


Your doctor will tell you when you can start taking HRT again.





Effects on your risk of developing cancer



Breast cancer:



Women who have breast cancer, or have had breast cancer in the past, should not take HRT.


Taking HRT slightly increases the risk of breast cancer; as does having a later menopause. Your risk of breast cancer is also higher if you:


  • have a close relative (mother, sister or grandmother) who has had breast cancer

  • are seriously overweight.

The risk for a post-menopausal woman taking estrogen-only HRT for 5 years is about the same as for a woman of the same age who is still having periods over that time and not taking HRT. The risk for a woman who is taking estrogen plus progestogen HRT is higher than for estrogen-only HRT (but estrogen plus progestogen HRT is beneficial for the endometrium, see 'Endometrial cancer' below).


For all kinds of HRT, the extra risk of breast cancer increases the longer you take it, but returns to normal within about 5 years after stopping.




Compare


Looking at women aged 50 who are not taking HRT - on average, 32 in 1000 will be diagnosed with breast cancer by the time they reach the age of 65.


For women who start taking estrogen-only HRT at age 50 and take it for 5 years, the figure will be between 33 and 34 in 1000 (ie an extra 1-2 cases).


If they take estrogen-only HRT for 10 years, the figure will be 37 in 1000 (ie an extra 5 cases).


For women who start taking estrogen plus progestogen HRT at age 50 and take it for 5 years, the figure will be 38 in 1000 (ie an extra 6 cases).


If they take estrogen plus progestogen HRT for 10 years, the figure will be 51 in 1000 (ie an extra 19 cases)




If you notice any changes in your breasts, such as:


  • dimpling of the skin

  • changes in the nipple

  • any lumps you can see or feel


Make an appointment to see your doctor as soon as possible.



Endometrial cancer (cancer of the lining of the womb):



Taking estrogen-only HRT for a long time can increase the risk of cancer of the lining of the womb (the endometrium). Taking a progestogen as well as the estrogen helps to lower the extra risk.


Elleste Solo is an estrogen-only product.



If you still have your womb, your doctor may prescribe a progestogen as well as estrogen. If so, these may be prescribed separately, or as a combined HRT product.



If you have had your womb removed (a hysterectomy), your doctor will discuss with you whether you can safely take estrogen without a progestogen.



If you've had your womb removed because of endometriosis, any endometrium left in your body may be at risk. So your doctor may prescribe HRT that includes a progestogen as well as an estrogen.




Compare


Looking at women who still have a uterus and who are not taking HRT - on average 5 in 1000 will be diagnosed with endometrial cancer between the ages of 50-65.


For women who take estrogen-only HRT, the figure will be between 10 and 60 in 1000 (ie an extra 5 to 55 cases), depending on the dose and how long you take it.


The addition of a progestogen to estrogen-only HRT substantially reduces the risk of endometrial cancer.



If you get breakthrough bleeding or spotting, it's usually nothing to worry about, especially during the first few months of taking HRT.




Make an appointment to see your doctor if the bleeding or spotting:


  • carries on for more than the first few months

  • starts after you've been on HRT for a while

  • carries on even after you've stopped taking HRT

  • It could be a sign that your endometrium has become thicker.


Ovarian cancer


Ovarian cancer (cancer of the ovaries) is very rare, but it is serious. It can be difficult to diagnose, because there are often no obvious signs of the disease.


Some studies have indicated that taking estrogen-only HRT for more than 5 years may increase the risk of ovarian cancer. It is not yet known whether other kinds of HRT increase the risk in the same way.





While you are taking Elleste Solo


Certain diseases sometimes get worse when you are taking hormone replacement therapy. Your doctor may need to check you more closely if you have any of the following.


  • Migraine or severe headache

  • Asthma

  • Gallstones

  • Epilepsy

  • High blood pressure

  • A personal or family history of blood clots

  • Diabetes (see below)

  • Liver problems

  • Heart or kidney problems

  • Endometrial hyperplasia (overgrowth of the lining of your womb)

  • Fibroids in your womb (see below)

  • Endometriosis (where tissue from your womb is found outside the womb)

  • A history of breast cancer in your family

  • Systemic lupus erythematosus (SLE; a chronic inflammatory disease affecting the skin and organs)

  • Otosclerosis (an inherited form of deafness which sometimes gets worse during pregnancy)

  • High levels of lipids in your blood (hypertriglyceridaemia)

Elleste Solo may affect the result of certain laboratory tests, so tell the person taking the sample that you are taking Elleste Solo.


If you have:



  • fibroids (lumps of fibrous and muscular tissue) in your womb, these may increase in size when you are taking Elleste Solo. See your doctor if you have pain or swelling in your abdomen.


  • diabetes, you may need to change the amount of insulin you take. Check your blood glucose level more often until it is steady.


Do i need to use contraception while I am taking Elleste Solo ?


It is important to remember that Elleste Solo is not a contraceptive (the pill).


If you are using the pill or another hormonal contraceptive you will need to use another type of contraceptive. Please discuss this with your doctor.





Taking other medicines with Elleste Solo


Please tell your doctor or pharmacist if you are using or have recently used any other medicines, including over-the-counter medicines.


In particular, tell your doctor if you are using any of the following because they may alter the effects of Elleste Solo:


  • drugs that treat epilepsy, and some anti-infectives (anti-virals and antibiotics) and sedatives.

  • herbal medicines containing St. John's Wort.


  • diabetic drugs, as this product may affect your blood glucose level. If you are being treated for diabetes please let your doctor or pharmacist know that you take Elleste Solo.

If your doctor does not know that your are taking these other medicines, tell him or her before you start taking Elleste Solo.





Pregnancy and breast-feeding


Elleste Solo is for use in post-menopausal women. It should not be taken by pregnant or breast-feeding women.





Driving or using machines


No effects on driving or using machinery have been observed for Elleste Solo.





Important information about some of the ingredients of Elleste Solo Tablets


Elleste Solo contains lactose. If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.



Sunset yellow colouring in Elleste Solo 2mg can cause allergic-type reactions, including asthma. This allergy is more common in people who are allergic to aspirin.





How To Take Elleste Solo



If you are still having regular periods, take your first tablet on the first day of bleeding.



If you are not having regular periods, you can start straight away.


  • Take one tablet each day. You can take the tablet at a time of the day that suits you. But it is best to take it about the same time each day.

  • Swallow the tablets whole, with some water.

  • Follow the direction of the arrows on the pack and take a tablet each day until the pack is empty. All the tablets are the same.

  • The days of the week are marked on the strip to help you to remember to take one each day.

  • When you finish a foil strip, start a new strip on the next day.


Changing from another type of HRT


If you are changing from another type of HRT, start taking Elleste Solo when you finish the pack of HRT you are taking at the moment.


If your doctor gives you instructions on changing from another type of HRT you should follow these instructions. If you have any doubts you should contact your doctor.



Will I have periods?


If you have not had a hysterectomy, and you are also taking a progestogen, you will probably have a monthly bleed. In the first few months you may get irregular bleeding. However, if this carries on you should tell your doctor.




If you forget to take a tablet


Take the tablet as soon as you remember, and take the next one at the normal time.


If you have missed your tablet by more than 12 hours, dispose of this tablet safely and take the next one at the normal time. If you have not had a hysterectomy you may experience breakthrough bleeding or spotting.





If you take more than you should


There should be no problems, but you may feel sick or actually be sick. If you are worried contact your doctor. Take the usual table the following day.





Possible Side Effects


Like all medicines, Elleste Solo can cause side effects, although not everybody gets them. If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.



Stop taking the tablets immediately and tell your doctor if:


  • you become jaundiced (yellowing of the skin or eyes);

  • you have itching all over your body;

  • you have an unusual, severe or prolonged headache;

  • your sight is affected in any way;

  • you find it difficult to speak;

  • any part of your body suddenly feels weak or numb;

  • there is a chance that you could be or could become pregnant; or

  • you develop any of the conditions listed under "Before you take Elleste Solo".


During the first few months you may feel sick, have headaches, or your breasts may be painful or increase in size. These side effects should lessen as your body gets used to the medicine.




You may also get the following side effects:



Common: feeling sick, stomach cramps, headache, an increase in size of fibroids in the womb, breakthrough bleeding, changes in weight, oedema (swelling) of legs, breast tenderness and enlargement, mood changes, changes in sex drive.



Uncommon: indigestion, being sick, flatulence, gallstones and gallbladder disease, feeling dizzy, migraine, vaginal thrush, increase in blood pressure, leg cramps, breast cancer (please refer to the earlier section on breast cancer).



Rare: loss of hair from the scalp, increase in body and facial hair, itchiness, rashes, thromboembolic disease (please refer to the earlier section on the effects of HRT on the heart and circulation).



Very rare: heart disease (please refer to the earlier section on the effects of HRT on the heart and circulation), stroke, chloasma (brown patches on the skin), red swellings on the skin.


HRT will not prevent memory loss. In one study of women who started using combined HRT after the age of 65, a small increase in the risk of dementia was observed.





How To Store Elleste Solo


Keep out of the reach and sight of children.


Do not store above 25°C. Store in the original package.


Don't take Elleste Solo after the 'expiry date' shown on the box.


If your tablets are out of date, take them to your pharmacist who will dispose of them safely.




Further Information



What Elleste Solo contains


  • Elleste Solo 1mg tablets contain the active ingredient 1 milligram estradiol (as hemihydrate).

  • Elleste Solo 2mg tablets contain the active ingredient 2 milligrams estradiol (as hemihydrate).

    (The estradiol hemihydrate used to make Elleste Solo does not come from animals).

  • The tablets also contain: lactose monohydrate, maize starch, povidone, talc, magnesium stearate, macrogol 400, titanium dioxide (E171), and hypromellose (E464).

  • Elleste Solo 2mg has the extra ingredient sunset yellow (E110) (see also the warning at the end of section 2).



What Elleste Solo looks like and contents of the pack


Elleste Solo 1mg tablets are white film-coated tablets with an embossing.


Elleste Solo 2mg tablets are orange film-coated tablets with an embossing.


They are supplied in three blister strips in each pack. Each strip contains 28 tablets.




Marketing Authorisation Holder



Meda Pharmaceuticals Ltd

Skyway House

Parsonage Road

Takeley

Bishop's Stortford

CM22 6PU

UK




Manufacturer



Piramal Healthcare UK Ltd.

Whalton Road

Morpeth

Northumberland

NE61 3YA

UK




This leaflet was last approved in
October 2009.


If you have any comments on the way this leaflet is written, please write to



Meda Pharmaceuticals Ltd

Skyway House

Parsonage Road

Takeley

Bishop's Stortford

CM22 6PU

UK


5012/PIL6 5013/PIL6


20701187





Sentinel Flavor Tabs





Dosage Form: FOR ANIMAL USE ONLY
Sentinel Flavor Tabs

SENTINEL® (milbemycin oxime/lufenuron) Flavor Tabs®


The palatable once-a-month prescription tablet that prevents heartworm disease and flea populations in dogs and puppies. SENTINEL® (milbemycin oxime/lufenuron) Flavor Tabs® also control flea populations and adult hookworms, and remove and control adult roundworm and whipworm infection in dogs and puppies.



Caution


Federal (USA) law restricts this drug to use by or on the order of a licensed veterinarian.



Warnings


Not for human use. Keep this and all drugs out of the reach of children.



Description


Sentinel Flavor Tabs are available in four tablet sizes in color-coded packages for oral administration to dogs and puppies according to their weight. (See Dosage Section). Each tablet is formulated to provide a minimum of 0.23 mg/pound (0.5 mg/kg) of milbemycin oxime and 4.55 mg/pound (10 mg/kg) body weight of lufenuron.


Milbemycin oxime consists of the oxime derivatives of 5-didehydromilbemycins in the ratio of approximately 80% A4 (C32H45NO7, MW 555.71) and 20% A3 (C31H43NO7, MW 541.68). Milbemycin oxime is classified as a macrocyclic anthelmintic.


Lufenuron is a benozylphenylurea derivative with the following chemical composition: N-[2,5-dichloro-4-(1,1,2,3,3,3, - hexafluoropropoxy)-phenylaminocarbonyl]-2,6- difluorobenzamide (C17H8Cl2F8N2O3, MW 511.15). Benzozylphenylurea compounds, including lufenuron, are classified as insect development inhibitors (IDIs).



Mode of Action


Milbemycin oxime, one active ingredient in Sentinel Flavor Tabs, is a macrocyclic anthelmintic which is believed to act by interfering with invertebrate neurotransmission. Milbemycin oxime eliminates the tissue stage of heartworm larvae and the adult stage of hookworm (Ancylostoma caninum), roundworm (Toxocara canis and Toxascaris leonine) and whipworm (Trichuris vulpis) infestations when administered orally according to the recommended dosage schedule.


Lufenuron, the other active ingredient, Sentinel Flavor Tabs, is an insect development inhibitor which breaks the flea life cycle by inhibiting egg development. Lufenuron’s mode of action is interference with chitin synthesis, polymerization and deposition. Lufenuron has no effect on the adult flea. After biting a lufenuron-treated dog, the female flea ingests a blood meal containing lufenuron which is subsequently deposited in her eggs. Lufenuron prevents most flea eggs from hatching or maturing into adults and thus prevents and controls flea populations by breaking the life cycle. (See Efficacy).



Indications


Sentinel Flavor Tabs are indicated for use in dogs and puppies, four weeks of age and older, and two pounds body weight or greater. Sentinel Flavor Tabs are also indicated for the prevention of heartworm disease caused by Dirofilaria immitis, for the prevention and control of flea populations, the control of adult Ancylostoma caninum (hookworm), and the removal and control of adult Toxocara canis and Toxocara leonina (roundworm) and Trichuris vulpis (whipworm) infections.


Lufenuron controls flea populations by preventing the development of flea eggs and does not kill adult fleas. Concurrent use of adulticide product may be necessary for adequate control of adult fleas.


Sentinel Flavor Tabs may be used con currently with CAPSTAR® (nitenpyram) Tablets to provide a Flea Management System that kills adult fleas and prevents flea eggs from hatching. Please see the Supplemental Veterinary Package Insert provided with this product for information about concurrent use of the two products,


Without concurrent use of an adulticide, adequate flea control may not be achieved in dogs that have repeated exposure to flea infested animals or environments.



Precautions


Do not use in puppies less than four weeks of age and less than two pounds of body weight. Prior to administration of Sentinel Flavor Tabs, dogs should be tested for existing heartworm infections. Infected dogs should be treated to remove adult heartworms and microfilariae prior to initiating treatment with Sentinel Flavor Tabs. Mild, transient hypersensitivity reactions manifested as labored respiration, vomiting, salivation and lethargy have been noted in some treated dogs carrying a high number of circulating microfilariae. These reactions are presumably caused by release of protein from dead or dying microfilariae.


Sentinel Flavor Tabs immediately break the flea life cycle by inhibiting egg development. However, pre-existing flea populations may continue to develop and emerge after treatment with Sentinel Flavor Tabs has begun. Based on results of clinical studies, this emergence generally occurs during the first 30-60 days. Therefore, noticeable control may not be observed until several weeks after dosing when a pre-existing infestation is present. Cooler geographic areas may have longer lag periods due to a prolonged flea life cycle. The concurrent use of an approved adulticide, like CAPSTAR may be employed depending on the severity of the infestation.


If a Sentinel Flavor Tabs-treated dog comes in contact with a flea-infested environment, adult fleas may infest the treated animal. These adult fleas are unable to produce viable offspring. The temporary use of an adulticide product may be necessary to kill these adult fleas.



Efficacy: Milbemycin Oxime


Milbemycin oxime provided complete protection against heartworm infection in both controlled laboratory and clinical trials.


In laboratory studies, a single dose of milbemycin oxime at 0.5 mg/kg was effective in removing roundworm, hookworm and whipworm. In well-controlled clinical trials, milbemycin oxime was also effective in removing roundworms and whipworms and in controlling hookworms.



Efficacy: Lufenuron


Lufenuron provided 99% control of flea egg development for 32 days following a single dose of lufenuron at 10 mg/kg in studies using experimental flea infestations. In well-controlled clinical trials, when treatment with lufenuron tablets was initiated prior to the flea season, mean flea counts were lower in lufenuron-treated dogs versus placebo-treated dogs. After 6 monthly treatments, the mean number of fleas on lufenuron-treated dogs was approximately 4 compared to 230 on placebo-treated dogs.


When treatment was initiated during the flea season, lufenuron tablets were effective in controlling flea infestations on dogs that completed the study. The mean flea count per lufenuron-treated dog was approximately 74 prior to treatment but had decreased to 4 after six monthly doses of lufenuron. A topical adulticide was used in the first eight weeks of the study to kill the pre-existing adult fleas.



Safety: Milbemycin Oxime


Milbemycin oxime has been tested safely in over 75 different breeds of dogs, including collies, pregnant females, breeding males and females, and puppies over two weeks of age. In well-controlled clinical field studies 786 dogs completed treatment with milbemycin oxime. Milbemycin oxime was used safely in animals receiving frequently used veterinary products such as vaccines, anthelmintics, antibiotics, steroids, flea collars, shampoos, and dips.


Two studies in heartworm-infected dogs were conducted which demonstrated mild, transient hypersensitivity reactions in treated dogs with high microfilaremia counts (see Precautions for reactions observed). Safety studies in pregnant dogs demonstrated that high doses (1.5 mg/kg = 3X) of milbemycin oxime given in an exaggerated dosing regimen (daily from mating through weaning), resulted in measurable concentrations of the drug in milk. Puppies nursing these females which received exaggerated dosing regimens demonstrated milbemycin-related effects. These effects were directly attributable to the exaggerated experimental dosing regime. The product is normally intended for once-a-month administration only. Subsequent studies included using 3X daily from mating to one week before weaning and demonstrated no effects on the pregnant females or their litters. A second study where pregnant females were dosed once at 3X the monthly use rate either before, on the day of or shortly after whelping resulted in no effects on the puppies.


Some nursing puppies, at 2, 4, and 6 weeks of age, given greatly exaggerated oral doses of milbemycin oxime (9.6 mg/kg = 19X) exhibited signs typified by tremors, vocalization and ataxia. These effects were all transient and puppies returned to normal within 24 to 48 hours. No effects were observed in puppies given the recommended dose of milbemycin oxime (0.5 mg/kg). This product has not been tested in dogs less than 2.2 pounds in body weight.


A rising-dose safety study conducted in rough-coated collies manifested a clinical reaction consisting of ataxia, pyrexia and periodic recumbency in one of fourteen dogs treated with milbemycin oxime at 12.5 mg/kg (25X monthly use rate). Prior to receiving the 12.5 mg/kg dose (25X monthly use rate) on day 56 of the study, all animals had undergone an exaggerated dosing regimen consisting of 2.5 mg/kg milbemycin oxime (5X monthly use rate) on day 0, followed by 5.0 mg/kg (10X monthly use rate) on day 14 and 10.0 mg/kg (20X monthly use rate) on day 32. No adverse reactions were observed in any of the collies treated with this regimen up through the 10.0 mg/kg (20X monthly use rate) dose.



Safety: Lufenuron


Lufenuron tablets have been used and tested safely in over forty breeds of dogs, including pregnant females, breeding males and puppies over six weeks of age. In well-controlled clinical trials, 151 dogs completed treatment with lufenuron tablets. Lufenuron tablets were used safely in animals receiving frequently used veterinary products such as vaccines, anthelmintics, antibiotics and steroids. In a ten-month study, doses up to 10X the recommended dose rate of 10 mg/kg caused no overt toxicity. A single dose of 200 mg/kg (20X the recommended dose rate) had no marked effect on adult dogs, but caused decreased activity and appetite in eight week old puppies. Mean body weights of male and female puppies were higher in treated versus control group at the end of the study. In specifically designed target animal safety studies, lufenuron tablets were tested with concurrent administration of flea adulticids containing carbaryl, permethrin, chlorpyriphos and cythioate. No toxicity resulted from these combinations. Lufenuron tablets did not cause cholinesterase inhibition nor did they enhance cholinesterase inhibition caused by exposure to organophosphates.


Four reproductive safety studies were conducted in breeding dogs with lufenuron tablets: two laboratory and two well-controlled clinical studies. In one of the laboratory studies, where lufenuron was administered to beagle dogs at doses equivalent to 90X (3X daily) the monthly recommended dose of 10 mg/kg, the ratio of gravid females to females mated was 8/8 or 100% in the control group and 6/9 or 67% in the lufenuron-treated group. The mean number of pups per litter was two animals higher in the treated versus control groups and the mean birth weights of pups from treated bitches in this study was lower than control groups.


These pups grew at a similar rate to control pups. There was a higher incidence of four clinical signs in the lufenuron-treated versus control group: nasal discharge, pulmonary congestion, diarrhea/dehydration and sluggishness. The incidence of these signs was transient and decreasing by the end of lactation. Results from three additional reproductive safety studies, one laboratory and two clinical field studies evaluating eleven breeds of dogs, did not demonstrated any adverse finding for the reproductive parameters measured including fertility, pup birth weights and pup clinical signs after administration of lufenuron up to 5X the recommended monthly use rate.


Data from analysis of milk from lactating animals treated with lufenuron tablets of 2X and 6X the recommended monthly use rate demonstrates that lufenuron concentrates in the milk of these dogs. The average milk: blood concentration ratio was approximately 60 (i.e., 60X higher drug concentrations in the milk compared to drug levels in the blood of treated bitches). Nursing puppies averaged 8-9 times higher blood concentrations of lufenuron compared to their dams.



Dosage


Sentinel Flavor Tabs are given orally, once a month, at the recommended minimum dosage of 0.23 mg/lb (0.5 mg/kg) milbemycin oxime and 4.55 mg/lb (10 mg/kg) lufenuron.


Dogs over 100 lbs are provided the appropriate combination of tablets.


*Please see separate insert in this package for concurrent dosing of Sentinel Flavor Tabs and CAPSTAR Tablets



Administration



TO ENSURE ADEQUATE ABSORPTION, ALWAYS ADMINISTER Sentinel Flavor Tabs TO DOGS IMMEDIATELY AFTER OR IN CONJUNCTION WITH A NORMAL MEAL.
















Recommended Dosage Schedule
Body WeightMilbemycin Oxime Per TabletLufenuron Per Tablet
2 to 10 lbs.2.3 mg46.0 mg
11 to 25 lbs.5.75 mg115 mg
26 to 50 lbs.11.5 mg230 mg
51 to 100 lbs.23.0 mg460 mg

Sentinel Flavor Tabs are palatable and most dogs will consume the tablet when offered by the owner. As an alternative to direct dosing, the tablets can be hidden in food. Be certain the dog consumes the entire tablet or tablets. Administer Sentinel Flavor Tabs to dogs immediately after or in conjunction with a normal meal. Food is essential for adequate absorption of lufenuron. Watch the dog closely following administration to be sure the entire dose have been consumed. If it is not entirely consumed, redose with the full recommended dose as soon as possible.


Sentinel Flavor Tabs must be administered monthly, preferably on the same date each month. Treatment with Sentinel Flavor Tabs may begin at any time of year. In geographic areas where mosquitoes and fleas are seasonal, the treatment schedule should begin one month prior to the expected onset and should continue until the end of “mosquito and flea season.” In areas with year-round infestations, treatment should continue through the entire year without interruption.


If a dose is missed and a 30-day interval between dosing is exceeded, administer Sentinel Flavor Tabs immediately and resume the monthly dosing schedule. If Sentinel Flavor Tabs replace daily diethylcarbamazine (DEC) for heartworm prevention, the first dose must be given within 30 days after the last dose of DEC.



Adverse Reactions


The following adverse reactions have been reported in dogs after giving milbemycin oxime or lufenuron: vomiting, depression/lethargy, pruitus, urticaria, diarrhea, anorexia, skin congestion, ataxia, convulsions, hypersalivation and weakness.



How Supplied


Sentinel Flavor Tabs are available in four tablet sizes, (see Dosage Section), formulated according to the weight of the dog. Each tablet size is available in color-coded packages of 6 or 12 tablets each, which are packaged 10 per display carton.



Storage Conditions


Store in a dry place at controlled room temperature, between 59º and 77ºF (15-25ºC).


Questions? Comments? Please Call 1-800-332-2761


Visit our website at www.petwellness.com


Manufactured for:      


Novartis Animal Health US, Inc.

Greensboro, NC 27408


NADA #141-084, Approved by FDA


©2007 Novarits Animal Health US, Inc.


SENTINEL, Flavor Tabs and CAPSTAR are registered trademarks of Novartis AG.



SENTINEL® (milbemycin oxime/lufenuron) Flavor Tabs®        Capstar® (nitenpyram)


FLEA MANAGEMENT SYSTEM


Supplemental Veterinary Package Insert


This insert describes the concurrent use of SENTINEL® (milbemycin oxime/lufenuron) Flavor Tabs® and CAPSTAR® (nitenpyram) Tablets for the management of fleas on dogs and puppies. Please read the insert contained in each package for complete information of the individual products prior to dispensing or dosing. The effects of Sentinel Flavor Tabs on heartworm disease and internal parasites are not described in this supplement.



Caution


Federal (USA) law restricts this drug to use by or on the order of a licensed veterinarian.



Warnings


Not for human use. Keep this and all drugs out of the reach of children.



Indications


In dogs and puppies, the concurrent use of Sentinel Flavor Tabs and CAPSTAR Tablets is indicated to kill adult fleas and prevent eggs from hatching. The effects of Sentinel Flavor Tabs, which prevent and control flea populations, and CAPSTAR Tablets, which treat flea infestations are combined to provide a FLEA MANAGEMENT SYSTEM.



Step 1: Control


Give Sentinel Flavor Tabs once per month to prevent and control flea populations. Sentinel Flavor Tabs contain lufenuron. Lufenuron controls flea populations by preventing the development of flea eggs and does not kill adult fleas. If a dog currently has a flea infestation, more rapid relief can be accomplished by adding CAPSTAR to the treatment as follows.



Step 2: Kill Adult Fleas


If your pet Currently has a flea infestation, add CAPSTAR Tablets to kill adult fleas. CAPSTAR Tablets contain nitenpyram and are effective for treatment of flea infestations. Nitenpyram starts killing adult fleas within 30 minutes of administration.


  • Administer CAPSTAR Tablets once per week until adult fleas are no longer observed.

  • For a severe flea infestation, administer CAPSTAR Tablets twice per week until adult fleas are no longer observed.

  • Additional CAPSTAR Tablets may be administered as needed to kill the occasional adult flea picked up from infested environments.

  • It is important to treat all cats and dogs in the household. All cats should be treated with approved products like lufenuron in combination with nitenpyram as needed. Fleas can reproduce on untreated pets and allow infestations to persist.


Dosage


The combination of Sentinel Flavor Tabs and CAPSTAR Tablets should be administered according to the following schedule. Weigh your dog prior to administration to ensure proper dosage. Do not administer to dogs under 2 pounds.



























Recommended Dosage Schedule
Body WeightDoseCAPSTAR Once or twice weekly* (Nitenpyram per tablet)Sentinel Flavor Tabs once per month (Lufenuron per tablet)
2 to 10 lbs.One Tablet11.446.0 mg
11 to 25 lbs.One Tablet11.4115 mg
26 to 50 lbs.One Tablet57.0230 mg
51 to 100 lbs.One Tablet57.0460 mg
101 to 125 lbs.One Tablet57.0**

*If adult fleas are seen


**Dogs over 100 lbs. are provided the appropriate combination of Sentinel Flavor Tabs.



Precautions


The safety of the concurrent use of Sentinel Flavor Tabs and CAPSTAR Tablets in pregnant or nursing dogs or in puppies less than 11 weeks of age has not been demonstrated.



Adverse Reactions


The following adverse reactions have been reported in dogs after giving Sentinel Flavor Tabs: vomiting, depression/lethargy, pruritus, urticaria, diarrhea, anorexia, skin congestion, ataxia, convulsions, hypersalivation and weakness.



Effectiveness


Please refer to the labeling for Sentinel Flavor Tabs and CAPSTAR Tablets for information about the effectiveness of each product. Studies testing the concurrent use of the two products demonstrated that each product remains effective for its labeled indication when both are administered concurrently. In a simulated home environment, the administration of Sentinel Flavor Tabs monthly and CAPSTAR either once or twice weekly demonstrated a greater and more rapid reduction of established flea infestations than Sentinel Flavor Tabs alone.



Animal Safety


The combination of nitenpyram, milbemycin oxime and lufenuron has been tested in a 90 day laboratory study. Administration of 5X the recommended use rate of CAPSTAR Tablets for 90 consecutive days, concurrently with administration of 5X the recommended use rate of Sentinel Flavor Tabs every 2 weeks for 7 treatments was well tolerated.



Flea Infestations on Dogs


In addition to the common nuisance irritations associated with infestations, fleas can be responsible for skin conditions in the dog such as flea allergy dermatitis. Fleas also transmit other parasites, including tapeworms. The control of flea infestations reduces the problems associated with these parasites.


Sentinel Flavor Tabs break the flea life cycle by inhibiting egg development. CAPSTAR Tablets rapidly kill adult fleas on the dog. The concurrent use of these two products provides an effective flea management system.


The following diagram illustrates the flea’s life cycle and where the combination of Sentinel Flavor Tabs and CAPSTAR Tablets work:


Life Cycle of the Flea



A single female flea may produce up to 2,000 eggs over her lifetime. Eggs hatch and can develop into adults within only three weeks. Adult female fleas feed by ingesting blood from the pet and subsequently lay eggs, which drop off the pet’s coat. Within days, larvae hatch from the eggs and live undetected in the pet’s surroundings, such as the carpet and bedding. Flea larvae spin a cocoon, and when appropriately stimulated, a young adult flea emerges and jumps onto the pet to continue the life cycle.


After reading this insert, if you have any questions about the concurrent use of Sentinel Flavor Tabs and CAPSTAR Tablets for your patients, please call Novartis Animal Health US, Inc. Veterinary Product Support at 1 (800)-332-2761.



Storage Conditions


Store Sentinel Flavor Tabs and CAPSTAR Tablets as described on the individual product inserts.


Questions? Comments?


Please Call 1-800-332-2761


Visit our website at www.petwellness.com


Manufactured for:      


Novartis Animal Health US, Inc.

Greensboro, NC 27408


NADA 141-204, Approved by FDA.


©2007 Novartis Animal Health US, Inc.


SENTINEL, Flavor Tabs and CAPSTAR are registered trademarks of Novartis AG.


NAH/SEN-FT/VIPI-FMS/2


12/07



PRINCIPAL DISPLAY PANEL


Package Label - 2.3 mg milbemycin oxime / 46 mg lufenuron


Recommended for dogs and puppies


2-10lbs.


NOVARTIS


ANIMAL HEALTH


Sentinel® flavor tabs® 


(milbemycin oxime • lufenuron)


Once-a-month flavored tablets


6 PACK


Give with a meal


 




PRINCIPAL DISPLAY PANEL


Package Label - 5.75 mg milbemycin oxime / 115 mg lufenuron


Recommended for dogs and puppies


11-25lbs.


NOVARTIS


ANIMAL HEALTH


Sentinel® flavor tabs® 


(milbemycin oxime • lufenuron)


Once-a-month flavored tablets


6 PACK


Prevents Heartworm Disease


and Flea Populations in Dogs and Puppies


Also controls flea populations, adult hookworm


infections, removes and controls adult roundworm


and whipworm infections in dogs and puppies.


Keep this and all drugs out of the reach of children.


Net contents: 6 tablets, 5.75 mg milbemycin oxime


and 115 mg lufenuron each.


Give with a meal


Caution: Federal (USA) law restricts


this drug to use by or on the order


of a licensed veterinarian.


Product # 52221 NADA # 141-084


Approved by FDA




PRINCIPAL DISPLAY PANEL


Package Label – 11.5 mg milbemycin oxime / 230 mg lufenuron


Recommended for dogs and puppies


26-50lbs.


NOVARTIS


ANIMAL HEALTH


Sentinel® flavor tabs® 


(milbemycin oxime • lufenuron)


Once-a-month flavored tablets


6 PACK


Prevents Heartworm Disease


and Flea Populations in Dogs and Puppies


Also controls flea populations, adult hookworm


infections, removes and controls adult roundworm


and whipworm infections in dogs and puppies.


Keep this and all drugs out of the reach of children.


Net contents: 6 tablets, 11.5 mg milbemycin oxime


and 230 mg lufenuron each.


Give with a meal


Caution: Federal (USA) law restricts


this drug to use by or on the order


of a licensed veterinarian.


Product # 52231 NADA # 141-084


Approved by FDA




PRINCIPAL DISPLAY PANEL


Package Label – 23 mg milbemycin oxime / 460 mg lufenuron


NOVARTIS


ANIMAL HEALTH


Sentinel® flavor tabs® 


(milbemycin oxime • lufenuron)


Once-a-month flavored tablets


6 PACK


Prevents Heartworm Disease


and Flea Populations in Dogs and Puppies


Also controls flea populations, adult hookworm


infections, removes and controls adult roundworm


and whipworm infections in dogs and puppies.


Keep this and all drugs out of the reach of children.


Net contents: 6 tablets, 23 mg milbemycin oxime


and 460 mg lufenuron each.


Give with a meal


Caution: Federal (USA) law restricts


this drug to use by or on the order


of a licensed veterinarian.


Product # 52241 NADA # 141-084


Approved by FDA










Sentinel Flavor Tabs 
milbemycin oxime and lufenuron  tablet, coated










Product Information
Product TypePRESCRIPTION ANIMAL DRUGNDC Product Code (Source)58198-5221
Route of AdministrationORALDEA Schedule    











Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MILBEMYCIN OXIME (MILBEMYCIN OXIME)MILBEMYCIN OXIME2.3 mg
LUFENURON (LUFENURON)LUFENURON46 mg





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
ColorBROWNScoreno score
ShapePENTAGON (5 SIDED) (biconvnex bevel-edges)Size7mm
FlavorMEAT (beef flavor)Imprint CodeCD;CGV
Contains      






















Packaging
#NDCPackage DescriptionMultilevel Packaging
158198-5221-11 BLISTER PACK In 1 BOXcontains a BLISTER PACK
16 TABLET In 1 BLISTER PACKThis package is contained within the BOX (58198-5221-1)
258198-5221-32 BLISTER PACK In 1 BOXcontains a BLISTER PACK
26 TABLET In 1 BLISTER PACKThis package is contained within the BOX (58198-5221-3)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NADANADA14108401/05/2000







Sentinel Flavor Tabs 
milbemycin oxime and lufenuron  tablet, coated










Product Information
Product TypePRESCRIPTION ANIMAL DRUGNDC Product Code (Source)58198-5222
Route of AdministrationORALDEA Schedule    











Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MILBEMYCIN OXIME (MILBEMYCIN OXIME)MILBEMYCIN OXIME5.75 mg
LUFENURON (LUFENURON)LUFENURON115 mg





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
ColorBROWNScoreno score
ShapePENTAGON (5 SIDED) (biconvnex bevel-edges)Size10mm
FlavorMEAT (beef flavor)Imprint CodeGNG;CGV
Contains      






















Packaging
#NDCPackage DescriptionMultilevel Packaging
158198-5222-11 BLISTER PACK In 1 BOXcontains a BLISTER PACK
16 TABLET In 1 BLISTER PACKThis package is contained within the BOX (58198-5222-1)
258198-5222-32 BLISTER PACK In 1 BOXcontains a BLISTER PACK
26 TABLET In 1 BLISTER PACKThis package is contained within the BOX (58198-5222-3)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NADANADA14108401/05/2000







Sentinel Flavor Tabs 
milbemycin oxime and lufenuron  tablet, coated










Product Information
Product TypePRESCRIPTION ANIMAL DRUGNDC Product Code (Source)58198-5223
Route of AdministrationORALDEA Schedule    











Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MILBEMYCIN OXIME (MILBEMYCIN OXIME)MILBEMYCIN OXIME11.5 mg
LUFENURON (LUFENURON)LUFENURON230 mg





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
ColorBROWNScoreno score
ShapePENTAGON (5 SIDED) (biconvnex bevel-edges)Size12mm
FlavorMEAT (beef flavor)Imprint CodeGLG;CGV
Contains      






















Packaging
#NDCPackage DescriptionMultilevel Packaging
158198-5223-11 BLISTER PACK In 1 BOXcontains a BLISTER PACK
16 TABLET In 1 BLISTER PACKThis package is contained within the BOX (58198-5223-1)
258198-5223-32 BLISTER PACK In 1 BOXcontains a BLISTER PACK
26 TABLET In 1 BLISTER PACKThis package is contained within the BOX (58198-5223-3)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NADANADA14108401/05/2000







Sentinel Flavor Tabs 
milbemycin oxime and lufenuron  tablet, coated










Product Information
Product TypePRESCRIPTION ANIMAL DRUGNDC Product Code (Source)58198-5224
Route of AdministrationORALDEA Schedule    











Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MILBEMYCIN OXIME (MILBEMYCIN OXIME)MILBEMYCIN OXIME23 mg
LUFENURON (LUFENURON)LUFENURON460 mg





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
ColorBROWNScoreno score
ShapePENTAGON (5 SIDED) (biconvnex bevel-edges)Size16mm
FlavorMEAT (Beef flavor)Imprint CodeGKG;CGV
Contains      






















Packaging
#NDCPackage DescriptionMultilevel Packaging
158198-5224-11 BLISTER PACK In 1 BOXcontains a BLISTER PACK
16 TABLET In 1 BLISTER PACKThis package is contained within the BOX (58198-5224-1)
258198-5224-32 BLISTER PACK In 1 BOXcontains a BLISTER PACK
26 TABLET In 1 BLISTER PACKThis package is contained within the BOX (58198-5224-3)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NADANADA14108401/05/2000


Labeler - Novartis Animal Health US, Inc. (966985624)
Revised: 12/2009Novartis Animal Health US, Inc.