Gliserin-Kansuk-B may be available in the countries listed below.
Ingredient matches for Gliserin-Kansuk-B
Glycerol
Glycerol is reported as an ingredient of Gliserin-Kansuk-B in the following countries:
- Turkey
International Drug Name Search
Tuesday 27 July 2010
Monday 26 July 2010
Diethylpropion
Diethylpropion hydrochloride, USP is available for oral administration in immediate-release tablets containing 25 mg Diethylpropion hydrochloride. The inactive ingredients in each immediate-release tablet are: corn starch, lactose monohydrate, magnesium stearate, pregelatinized starch and tartaric acid. Diethylpropion hydrochloride is a sympathomimetic agent. The chemical name for Diethylpropion hydrochloride is 1-phenyl-2-diethyl-amino1-propanone hydrochloride and has empirical formula of C13H19NO•HCl. The molecular weight is 241.76.
Its chemical structure is:
Diethylpropion - Clinical Pharmacology
Diethylpropion hydrochloride is a sympathomimetic amine with some pharmacologic activity similar to that of the prototype drugs of this class used in obesity, the amphetamines. Actions include some central nervous system stimulation and elevation of blood pressure. Tolerance has been demonstrated with all drugs of this class in which these phenomena have been looked for.
Drugs of this class used in obesity are commonly known as "anorectics" or "anorexigenics." It has not been established, however, that the action of such drugs in treating obesity is primarily one of appetite suppression. For example, other central nervous system actions or metabolic effects may be involved.
Adult obese subjects instructed in dietary management and treated with "anorectic" drugs lose more weight on the average than those treated with placebo and diet, as determined in relatively short-term clinical trials.
The magnitude of increased weight loss of drug-treated patients over placebo-treated patients averages some fraction of a pound a week. However, individual weight loss may vary substantially from patient to patient. The rate of weight loss is greatest in the first weeks of therapy for both drug and placebo subjects and tends to decrease in succeeding weeks. The possible origins of the increased weight loss due to the various drug effects are not established. The amount of weight loss associated with the use of an "anorectic" drug varies from trial to trial, and the increased weight loss appears to be related in part to variables other than the drug prescribed, such as the physician/investigator relationship, the population treated, and the diet prescribed. Studies do not permit conclusions as to the relative importance of the drug and non-drug factors on weight loss.
The natural history of obesity is measured in years, whereas most studies cited are restricted to a few weeks duration; thus, the total impact of drug-induced weight loss over that of diet alone is unknown. Diethylpropion is rapidly absorbed from the GI tract after oral administration and is extensively metabolized through a complex pathway of biotransformation involving N-dealkylation and reduction. Many of these metabolites are biologically active and may participate in the therapeutic action of Diethylpropion hydrochloride. Due to the varying lipid solubilities of these metabolites, their circulating levels are affected by urinary pH. Diethylpropion and/or its active metabolites are believed to cross the blood-brain barrier and the placenta.
Diethylpropion and its metabolites are excreted mainly by the kidney. It has been reported that between 75 to 106% of the dose is recovered in the urine within 48 hours after dosing. Using a phosphorescence assay that is specific for basic compounds containing benzoyl group, the plasma half-life of the aminoketone metabolites is estimated to be between 4 to 6 hours.
Indications and Usage for Diethylpropion
Diethylpropion hydrochloride tablets, USP are indicated in the management of exogenous obesity as a short-term adjunct (a few weeks) in a regimen of weight reduction based on caloric restriction in patients with an initial body mass index (BMI) of 30 kg/m2 or higher and who have not responded to appropriate weight reducing regimen (diet and/or exercise) alone. Below is a chart of BMI based on various heights and weights. BMI is calculated by taking the patients weight, in kilograms (kg), divided by the patient's height, in meters (m), squared. Metric conversions are as follows: pounds divided by 2.2 = kg; inches x 0.0254 = meters.
| Body Mass Index (BMI), kg/m2 | ||||||
|---|---|---|---|---|---|---|
| Weight (pounds) | Height (feet, inches) | |||||
| 5’0” | 5’3” | 5’6” | 5’9” | 6’0” | 6’3” | |
| 140 | 27 | 25 | 23 | 21 | 19 | 18 |
| 150 | 29 | 27 | 24 | 22 | 20 | 19 |
| 160 | 31 | 28 | 26 | 24 | 22 | 20 |
| 170 | 33 | 30 | 28 | 25 | 23 | 21 |
| 180 | 35 | 32 | 29 | 27 | 25 | 23 |
| 190 | 37 | 34 | 31 | 28 | 26 | 24 |
| 200 | 39 | 36 | 32 | 30 | 27 | 25 |
| 210 | 41 | 37 | 34 | 31 | 29 | 26 |
| 220 | 43 | 39 | 36 | 33 | 30 | 28 |
| 230 | 45 | 41 | 37 | 34 | 31 | 29 |
| 240 | 47 | 43 | 39 | 36 | 33 | 30 |
| 250 | 49 | 44 | 40 | 37 | 34 | 31 |
The usefulness of agents of this class (see CLINICAL PHARMACOLOGY) should be measured against possible risk factors inherent in their use such as those described below. Diethylpropion hydrochloride tablets, USP are indicated for use as monotherapy only.
Contraindications
Pulmonary hypertension, advanced arteriosclerosis, hyperthyroidism, known hypersensitivity or idiosyncrasy to the sympathomimetic amines, glaucoma, severe hypertension. (See PRECAUTIONS.)
Agitated states.
Patients with a history of drug abuse.
Use in combination with other anorectic agents is contraindicated.
During or within 14 days following the administration of monoamine oxidase inhibitors, hypertensive crises may result.
Warnings
Diethylpropion hydrochloride tablets should not be used in combination with other anorectic agents, including prescribed drugs, over-the-counter preparations, and herbal products.
In a case-control epidemiological study, the use of anorectic agents, including Diethylpropion, was associated with an increased risk of developing pulmonary hypertension, a rare, but often fatal disorder. The use of anorectic agents for longer than 3 months was associated with a 23-fold increase in the risk of developing pulmonary hypertension. Increased risk of pulmonary hypertension with repeated courses of therapy cannot be excluded.
The onset or aggravation of exertional dyspnea, or unexplained symptoms of angina pectoris, syncope, or lower extremity edema suggest the possibility of occurrence of pulmonary hypertension. Under these circumstances, Diethylpropion hydrochloride tablets should be immediately discontinued, and the patient should be evaluated for the possible presence of pulmonary hypertension.
Valvular heart disease associated with the use of some anorectic agents such as fenfluramine and dexfenfluramine has been reported. Possible contributing factors include use for extended periods of time, higher than recommended dose, and/or use in combination with other anorectic drugs. Valvulopathy has been very rarely reported with Diethylpropion hydrochloride tablets monotherapy, but the causal relationship remains uncertain. The potential risk of possible serious adverse effects such as valvular heart disease and pulmonary hypertension should be assessed carefully against the potential benefit of weight loss. Baseline cardiac evaluation should be considered to detect preexisting valvular heart diseases or pulmonary hypertension prior to initiation of Diethylpropion hydrochloride tablets treatment. Diethylpropion hydrochloride tablets are not recommended in patients with known heart murmur or valvular heart disease. Echocardiogram during and after treatment could be useful for detecting any valvular disorders which may occur.
To limit unwarranted exposure and risks, treatment with Diethylpropion hydrochloride tablets should be continued only if the patient has satisfactory weight loss within the first 4 weeks of treatment (e.g., weight loss of at least 4 pounds, or as determined by the physician and patient).
Diethylpropion hydrochloride tablets are not recommended for patients who used any anorectic agents within the prior year.
If tolerance develops, the recommended dose should not be exceeded in an attempt to increase the effect; rather, the drug should be discontinued. Diethylpropion hydrochloride tablets may impair the ability of the patient to engage in potentially hazardous activities such as operating machinery or driving a motor vehicle; the patient should therefore be cautioned accordingly.
Prolonged use of Diethylpropion hydrochloride may induce dependence with withdrawal syndrome on cessation of therapy. Hallucinations have occurred rarely following high doses of the drug. Several cases of toxic psychosis have been reported following the excessive use of the drug and some have been reported in which the recommended dose appears not to have been exceeded. Psychosis abated after the drug was discontinued.
When central nervous system active agents are used, consideration must always be given to the possibility of adverse interactions with alcohol.
Precautions
General
Caution is to be exercised in prescribing Diethylpropion hydrochloride tablets for patients with hypertension or with symptomatic cardiovascular disease, including arrhythmias. Diethylpropion hydrochloride tablets should not be administered to patients with severe hypertension.
Reports suggest that Diethylpropion hydrochloride may increase convulsions in some epileptics. Therefore, epileptics receiving Diethylpropion hydrochloride tablets should be carefully monitored. Titration of dose or discontinuance of Diethylpropion hydrochloride tablets may be necessary.
The least amount feasible should be prescribed or dispensed at one time in order to minimize the possibility of overdosage.
Information for Patients
The patient should be cautioned about concomitant use of alcohol or other CNS-active drugs and Diethylpropion hydrochloride tablets. (See WARNINGS.) The patient should be advised to observe caution when driving or engaging in any potentially hazardous activity
Laboratory Tests
None
Drug Interactions
Because Diethylpropion hydrochloride tablets are monoamines, hypertension may result when this agent is used with monoamine oxidase (MAO) inhibitors. (See CONTRAINDICATIONS.)
Efficacy of Diethylpropion with other anorectic agents has not been studied and the combined use may have the potential for serious cardiac problems; therefore, the concomitant use with other anorectic agents is contraindicated.
Antidiabetic drug requirements (i.e., insulin) may be altered. Concurrent use with general anesthetics may result in arrhythmias. The pressor effects of Diethylpropion and those of other drugs may be additive when the drugs are used concomitantly; conversely, Diethylpropion may interfere with antihypertensive drugs (i.e., guanethidine, α-methyldopa). Concurrent use of phenothiazines may antagonize the anorectic effect of Diethylpropion.
Carcinogenesis, Mutagenesis, and Impairment of Fertility
No long-term animal studies have been done to evaluate Diethylpropion hydrochloride for carcinogenicity. Mutagenicity studies have not been conducted. Animal reproduction studies have revealed no evidence of impairment of fertility (see Pregnancy).
Pregnancy
Teratogenic Effects. Pregnancy Category B. Reproduction studies have been performed in rats at doses up to 1.6 times the human dose (based on mg/m2) and have revealed no evidence of impaired fertility or harm to the fetus due to Diethylpropion hydrochloride. There are, however, no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.
Spontaneous reports of congenital malformations have been recorded in humans, but no causal relationship to Diethylpropion has been established.
Non-Teratogenic Effects. Abuse with Diethylpropion hydrochloride during pregnancy may result in withdrawal symptoms in the human neonate.
Nursing Mothers
Since Diethylpropion hydrochloride and/or its metabolites have been shown to be excreted in human milk, caution should be exercised when Diethylpropion hydrochloride tablets are administered to a nursing woman.
Geriatric Use
Clinical studies of Diethylpropion hydrochloride tablets did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients. In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy.
This drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function.
Pediatric Use
Since safety and effectiveness in pediatric patients below the age of 16 have not been established, Diethylpropion hydrochloride tablets are not recommended for use in pediatric patients 16 years of age and under.
Adverse Reactions
Cardiovascular: Precordial pain, arrhythmia (including ventricular), ECG changes, tachycardia, elevation of blood pressure, palpitation and rare reports of pulmonary hypertension. Valvular heart disease associated with the use of some anorectic agents such as fenfluramine and dexfenfluramine, both independently and especially when used in combination, have been reported. Valvulopathy has been very rarely reported with Diethylpropion hydrochloride tablets monotherapy, but the causal relationship remains uncertain.
Central Nervous System: In a few epileptics an increase in convulsive episodes has been reported; rarely psychotic episodes at recommended doses; dyskinesia, blurred vision, overstimulation, nervousness, restlessness, dizziness, jitteriness, insomnia, anxiety, euphoria, depression, dysphoria, tremor, mydriasis, drowsiness, malaise, headache, and cerebrovascular accident
Gastrointestinal: Vomiting, diarrhea, abdominal discomfort, dryness of the mouth, unpleasant taste, nausea, constipation, other gastrointestinal disturbances
Allergic: Urticaria, rash, ecchymosis, erythema
Endocrine: Impotence, changes in libido, gynecomastia, menstrual upset
Hematopoietic System: Bone marrow depression, agranulocytosis, leukopenia
Miscellaneous: A variety of miscellaneous adverse reactions has been reported by physicians. These include complaints such as dysuria, dyspnea, hair loss, muscle pain, increased sweating, and polyuria.
Drug Abuse and Dependence
Diethylpropion hydrochloride is a schedule IV controlled substance. Diethylpropion hydrochloride has some chemical and pharmacologic similarities to the amphetamines and other related stimulant drugs that have been extensively abused. There have been reports of subjects becoming psychologically dependent on Diethylpropion. The possibility of abuse should be kept in mind when evaluating the desirability of including a drug as part of a weight reduction program. Abuse of amphetamines and related drugs may be associated with varying degrees of psychologic dependence and social dysfunction which, in the case of certain drugs, may be severe. There are reports of patients who have increased the dosage to many times that recommended. Abrupt cessation following prolonged high dosage administration results in extreme fatigue and mental depression; changes are also noted on the sleep EEG. Manifestations of chronic intoxication with anorectic drugs include severe dermatoses, marked insomnia, irritability, hyperactivity, and personality changes. The most severe manifestation of chronic intoxication is psychosis, often clinically indistinguishable from schizophrenia.
Overdosage
Manifestations of acute overdosage include restlessness, tremor, hyperreflexia, rapid respiration, confusion, assaultiveness, hallucinations, panic states, and mydriasis.
Fatigue and depression usually follow the central stimulation.
Cardiovascular effects include tachycardia, arrhythmias, hypertension or hypotension and circulatory collapse. Gastrointestinal symptoms include nausea, vomiting, diarrhea, and abdominal cramps. Overdose of pharmacologically similar compounds has resulted in convulsions, coma and death.
The reported oral LD50 for mice is 600 mg/kg, for rats is 250 mg/kg and for dogs is 225 mg/kg.
Management of acute Diethylpropion hydrochloride intoxication is largely symptomatic and includes lavage and sedation with a barbiturate. Experience with hemodialysis or peritoneal dialysis is inadequate to permit recommendation in this regard. Intravenous phentolamine (Regitine®) has been suggested on pharmacologic grounds for possible acute, severe hypertension, if this complicates Diethylpropion hydrochloride tablets overdosage.
Diethylpropion Dosage and Administration
Diethylpropion hydrochloride tablets:
One immediate-release 25 mg tablet three times daily, one hour before meals, and in midevening if desired to overcome night hunger.
Geriatric use: This drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function. (See PRECAUTIONS, Geriatric Use.)
How is Diethylpropion Supplied
Diethylpropion hydrochloride tablets USP, 25 mg are white, round tablets debossed cor over 208 on one side and plain on the other side. They are supplied as follows:
Bottles of 100 (NDC 64720-208-10)
Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].
Dispense in a tight container as defined in the USP.
Keep tightly closed.
Protect from excessive heat.
KEEP THIS AND ALL DRUGS OUT OF THE REACH OF CHILDREN
LB# 558 - 01 Rev. June, 2011
Manufactured and Distributed by:
CorePharma, LLC.
Middlesex, NJ 08846
PRINCIPAL DISPLAY PANEL
Diethylpropion HydrochlorideTablets
| Diethylpropion HYDROCHLORIDE Diethylpropion hydrochloride tablet | ||||||||||||||||||||
| ||||||||||||||||||||
| ||||||||||||||||||||
| ||||||||||||||||||||
| ||||||||||||||||||||
| ||||||||||||||||||||
| Marketing Information | |||
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| ANDA | ANDA040828 | 11/06/2008 | |
| Labeler - Corepharma LLC. (031192276) |
| Establishment | |||
| Name | Address | ID/FEI | Operations |
| Corepharma LLC. | 031192276 | ANALYSIS, LABEL, MANUFACTURE, PACK | |
More Diethylpropion resources
- Diethylpropion Side Effects (in more detail)
- Diethylpropion Dosage
- Diethylpropion Use in Pregnancy & Breastfeeding
- Drug Images
- Diethylpropion Drug Interactions
- Diethylpropion Support Group
- 51 Reviews for Diethylpropion - Add your own review/rating
- Diethylpropion MedFacts Consumer Leaflet (Wolters Kluwer)
- diethylpropion Advanced Consumer (Micromedex) - Includes Dosage Information
- Diethylpropion Hydrochloride Monograph (AHFS DI)
- Tenuate Consumer Overview
- Tenuate Dospan Controlled-Release Tablets MedFacts Consumer Leaflet (Wolters Kluwer)
Compare Diethylpropion with other medications
- Obesity
Friday 23 July 2010
Kapanol
Kapanol may be available in the countries listed below.
Ingredient matches for Kapanol
Morphine
Morphine sulphate pentahydrate (a derivative of Morphine) is reported as an ingredient of Kapanol in the following countries:
- Australia
- Belgium
- Bosnia & Herzegowina
- Germany
- Luxembourg
- Netherlands
- Switzerland
International Drug Name Search
Saturday 10 July 2010
Dep Gynogen
Generic Name: estradiol injection (ess tra DYE ol)
Brand Names: Clinagen LA 40, Delestrogen, Dep Gynogen, Depo-Estradiol, Estragyn LA 5, Gynogen LA 20, Menaval-20
What is Dep Gynogen (estradiol injection)?
Estradiol is a form of estrogen. Estrogen is a female sex hormone necessary for many processes in the body.
Estradiol injection is used to treat symptoms of menopause such as hot flashes, and vaginal dryness, burning, and irritation. It is also used to treat a lack of estrogen that is caused by ovarian failure or a condition called hypogonadism. Some forms of estradiol injection are used in men to treat the symptoms of prostate cancer.
Estradiol injection may also be used for other purposes not listed in this medication guide.
What is the most important information I should know about Dep Gynogen (estradiol injection)?
Do not use this medication if you have any of the following conditions: a history of stroke or blood clot, circulation problems, a hormone-related cancer such as breast or uterine cancer, or abnormal vaginal bleeding. This medication can cause birth defects in an unborn baby. Do not use if you are pregnant. Use an effective form of birth control, and tell your doctor if you become pregnant during treatment.
Estradiol increases your risk of developing endometrial hyperplasia, a condition that may lead to cancer of the uterus. Taking progestins while using estradiol may lower this risk. If your uterus has not been removed, your doctor may prescribe a progestin for you to take while you are using estradiol injection.
Long-term estradiol treatment may increase your risk of breast cancer, heart attack, or stroke. Talk with your doctor about your individual risks before using estradiol long-term. Your doctor should check your progress on a regular basis (every 3 to 6 months) to determine whether you should continue this treatment.
Have regular physical exams and self-examine your breasts for lumps on a monthly basis while using estradiol.
What should I discuss with my health care provider before using Dep Gynogen (estradiol injection)?
Do not use estradiol injection if you have:
a bleeding or blood-clotting disorder;
a history of stroke or circulation problems;
abnormal vaginal bleeding that a doctor has not checked; or
any type of breast, uterine, or hormone-dependent cancer.
Before using estradiol injection, tell your doctor if you have:
high blood pressure, angina, or heart disease;
high cholesterol or triglycerides;
- liver disease;
- kidney disease;
asthma;
epilepsy or other seizure disorder;
migraines;
diabetes;
depression;
gallbladder disease; or
if you have had your uterus removed (hysterectomy).
If you have any of these conditions, you may need a dose adjustment or special tests to safely use estradiol injection.
Estradiol increases your risk of developing endometrial hyperplasia, a condition that may lead to cancer of the uterus. Taking progestins while using estradiol may lower this risk. If your uterus has not been removed, your doctor may prescribe a progestin for you to take while you are using estradiol injection.
Long-term estradiol treatment may increase your risk of stroke. Talk with your doctor about your individual risks before using estradiol long-term. Your doctor should check your progress on a regular basis (every 3 to 6 months) to determine whether you should continue this treatment.
FDA pregnancy category X. This medication can cause birth defects. Do not use estradiol injection if you are pregnant. Tell your doctor right away if you become pregnant during treatment. Use an effective form of birth control while you are using this medication. Estradiol can pass into breast milk and may harm a nursing baby. This medication may also slow breast milk production. Do not use if you are breast-feeding a baby.
How should I use Dep Gynogen (estradiol injection)?
Use this medication exactly as it was prescribed for you. Do not use the medication in larger amounts, or use it for longer than recommended by your doctor. Follow the directions on your prescription label.
Estradiol injection is given as an shot into a muscle. You may be shown how to inject your medicine at home. Do not self-inject this medicine if you do not fully understand how to give the injection and properly dispose of used needles and syringes.
This medicine is usually given once every 4 weeks. Follow your doctor's instructions.
Do not draw your estradiol dose into a syringe until you are ready to give yourself an injection. Do not use the medication if it has changed colors or has any particles in it. Call your doctor for a new prescription.
Use each disposable needle only one time. Throw away used needles in a puncture-proof container (ask your pharmacist where you can get one and how to dispose of it). Keep this container out of the reach of children and pets.
Have regular physical exams and self-examine your breasts for lumps on a monthly basis while using estradiol injection.
Store this medication at room temperature away from moisture and heat.
What happens if I miss a dose?
Use the medication as soon as you remember. If it is almost time for the next dose, skip the missed dose and use the medicine at the next regularly scheduled time. Do not use extra medicine to make up the missed dose.
What happens if I overdose?
Seek emergency medical attention if you think you have used too much of this medicine. Overdose symptoms may include nausea, vomiting, or vaginal bleeding.
What should I avoid while using Dep Gynogen (estradiol injection)?
Follow your doctor's instructions about any restrictions on food, beverages, or activity while you are using estradiol injection.
Dep Gynogen (estradiol injection) side effects
Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Call your doctor at once if you have any of these serious side effects:
chest pain or heavy feeling, pain spreading to the arm or shoulder, nausea, sweating, general ill feeling;
sudden numbness or weakness, especially on one side of the body;
sudden headache, confusion, problems with vision, speech, or balance;
pain or swelling in your lower leg;
abnormal vaginal bleeding;
pain, swelling, or tenderness in your stomach;
jaundice (yellowing of the skin or eyes); or
a lump in your breast.
Less serious side effects may include:
nausea, vomiting, loss of appetite;
swollen breasts;
acne or skin color changes;
decreased sex drive, impotence, or difficulty having an orgasm;
migraine headaches or dizziness;
vaginal pain, dryness, or discomfort;
swelling of your ankles or feet;
depression; or
changes in your menstrual periods, break-through bleeding.
This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect. You may report side effects to FDA at 1-800-FDA-1088.
What other drugs will affect Dep Gynogen (estradiol injection)?
Before using estradiol injection, tell your doctor if you are using any of the following drugs:
St. John's wort;
phenobarbital (Luminal, Solfoton);
a blood thinner such as warfarin (Coumadin);
ritonavir (Norvir);
carbamazepine (Carbatrol, Tegretol);
rifampin (Rifadin, Rifater, Rifamate, Rimactane); or
antibiotics such as clarithromycin (Biaxin), erythromycin (E-Mycin, E.E.S., Erythrocin, Ery-Tab), ketoconazole (Nizoral), or itraconazole (Sporanox).
This list is not complete and there may be other drugs that can interact with estradiol injection. Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor.
More Dep Gynogen resources
- Dep Gynogen Side Effects (in more detail)
- Dep Gynogen Use in Pregnancy & Breastfeeding
- Dep Gynogen Drug Interactions
- Dep Gynogen Support Group
- 0 Reviews for Dep Gynogen - Add your own review/rating
- Estradiol Professional Patient Advice (Wolters Kluwer)
- Estradiol MedFacts Consumer Leaflet (Wolters Kluwer)
- estradiol Transdermal Advanced Consumer (Micromedex) - Includes Dosage Information
- Estradiol Monograph (AHFS DI)
- Estradiol Prescribing Information (FDA)
- Alora Prescribing Information (FDA)
- Alora Advanced Consumer (Micromedex) - Includes Dosage Information
- Climara Weekly Patch MedFacts Consumer Leaflet (Wolters Kluwer)
- Climara Prescribing Information (FDA)
- Climara Consumer Overview
- Delestrogen MedFacts Consumer Leaflet (Wolters Kluwer)
- Delestrogen Prescribing Information (FDA)
- Depo-Estradiol MedFacts Consumer Leaflet (Wolters Kluwer)
- Depo-Estradiol Prescribing Information (FDA)
- Estrace Prescribing Information (FDA)
- Estrace Advanced Consumer (Micromedex) - Includes Dosage Information
- Estrace MedFacts Consumer Leaflet (Wolters Kluwer)
- Estrace Consumer Overview
- Estraderm Patch MedFacts Consumer Leaflet (Wolters Kluwer)
- Estraderm Prescribing Information (FDA)
- Estradiol Patch Prescribing Information (FDA)
- Estrasorb Emulsion MedFacts Consumer Leaflet (Wolters Kluwer)
- Estrasorb Prescribing Information (FDA)
- Estrasorb Consumer Overview
- Evamist Prescribing Information (FDA)
- Evamist Consumer Overview
- Evamist Spray MedFacts Consumer Leaflet (Wolters Kluwer)
- Femring Prescribing Information (FDA)
- Femring Ring MedFacts Consumer Leaflet (Wolters Kluwer)
- Femtrace Advanced Consumer (Micromedex) - Includes Dosage Information
- Femtrace Prescribing Information (FDA)
- Femtrace MedFacts Consumer Leaflet (Wolters Kluwer)
- Femtrace Consumer Overview
- Menostar Weekly Patch MedFacts Consumer Leaflet (Wolters Kluwer)
- Menostar Prescribing Information (FDA)
- Menostar Consumer Overview
- Vivelle Prescribing Information (FDA)
- Vivelle-Dot Prescribing Information (FDA)
Compare Dep Gynogen with other medications
- Atrophic Urethritis
- Atrophic Vaginitis
- Breast Cancer, Palliative
- Hypoestrogenism
- Oophorectomy
- Osteoporosis
- Postmenopausal Symptoms
- Primary Ovarian Failure
- Prostate Cancer
Where can I get more information?
- Your pharmacist can provide more information about estradiol injection.
See also: Dep Gynogen side effects (in more detail)
Friday 9 July 2010
Betamed
In the US, Betamed is a member of the drug class vitamin and mineral combinations and is used to treat Vitamin/Mineral Supplementation and Deficiency.
Ingredient matches for Betamed
Betamethasone
Betamethasone 17α-valerate (a derivative of Betamethasone) is reported as an ingredient of Betamed in the following countries:
- Bahrain
- Oman
International Drug Name Search
Wednesday 7 July 2010
Baiweiha
Baiweiha may be available in the countries listed below.
Ingredient matches for Baiweiha
Loratadine
Loratadine is reported as an ingredient of Baiweiha in the following countries:
- China
International Drug Name Search
Saturday 3 July 2010
Alergoxal
Alergoxal may be available in the countries listed below.
Ingredient matches for Alergoxal
Cetirizine
Cetirizine dihydrochloride (a derivative of Cetirizine) is reported as an ingredient of Alergoxal in the following countries:
- Greece
International Drug Name Search
Subscribe to:
Posts (Atom)