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2nd presentation Oosterhuis AGAH
2nd presentation Oosterhuis AGAH

... – studies with single compound to obtain human PK in case of uncertain or conflicting animal/in vitro PK data – most studies comparing multiple candidates (up to 5) in parallel – design in most studies: parallel panels –> per compound oral-iv crossover in each panel – one 3-way crossover to compare ...
ranitidine (ra-ni-ti-deen) - DavisPlus
ranitidine (ra-ni-ti-deen) - DavisPlus

... ously for more than 2 wk without consulting health care professional. Notify health care professional if difficulty swallowing occurs or abdominal pain persists. Inform patient that smoking interferes with the action of histamine antagonists. Encourage patient to quit smoking or at least not to smok ...
Palliative Care in Winnipeg
Palliative Care in Winnipeg

... prescribe this substance, must be fully knowledgeable of the risks, benefits, potential complications, and drug ...
COLLEGE OF HEALTH SCIENCES
COLLEGE OF HEALTH SCIENCES

... Ascorbic acid is involved in metabolic hydroxylation and drug metabolism. T ( ) F ( ) ...
Doctor Discussion Guide
Doctor Discussion Guide

... than one-tenth of the binding affinity of the parent molecule for both the MT1 and MT2 receptors. ...
Bez nadpisu
Bez nadpisu

... • Administered as IV infusion: 3 mg/kg single dose followed with doses 2-6 weeks after the first dose, then q8weeks • Should be used with methotrexate for synergy and enhanced duration of response • Adverse events include increased risk of infection, hypersensitivity reactions, and formation of auto ...
Page Selective D3 receptor antagonist The dopamine D3
Page Selective D3 receptor antagonist The dopamine D3

... Previous studies in healthy volunteers demonstrated that GSK598809 (175 mg) is generally well tolerated (data on file). Adverse effects were assessed in 20 volunteers (10 males and 10 females) with a mean age of 32.8 years, mean weight of 73.5 kg and mean BMI of 23.6 kg/m 2 after an oral dose of 175 ...
Menstrual Discomfort
Menstrual Discomfort

... The prevalence of dysmenorrhoea is highest in adolescent women, with estimates ranging from 20% to 90% depending on the diagnosis standards applied [French, 2005]. For women dysmenorrhoea is the most common reason for absence from work. ...
VIROPTIC Solution, 1% Sterile Ophthalmic
VIROPTIC Solution, 1% Sterile Ophthalmic

... Although documented in vitro viral resistance to trifluridine has not been reported following multiple exposures to VIROPTIC, the possibility of the development of viral resistance exists. Carcinogenesis, Mutagenesis, Impairment of Fertility: Mutagenic Potential: Trifluridine has been shown to exer ...
Gemfibrozil is completely absorbed after oral administration of Lopid
Gemfibrozil is completely absorbed after oral administration of Lopid

... Gemfibrozil is completely absorbed after oral administration of Lopid tablets, reaching peak plasma concentrations 1 to 2 hours after dosing. Gemfibrozil pharmacokinetics are affected by the timing of meals relative to time of dosing. In one study (2), both the rate and extent of absorption of the d ...
PIO Nas - Badan Pengawas Obat dan Makanan
PIO Nas - Badan Pengawas Obat dan Makanan

... The recommended adult oral dosage is 0.1 mg of ramosetron hydrochloride once a day. Dosage may be adjusted depending on the patient’s age and symptoms. PRECAUTIONS 1. Important Precautions (1) Swallow with saliva or water : Nasea OD Tablet is not absorbed from the mucosa of the oral cavity, although ...
Glycopyrronium
Glycopyrronium

... glycopyrronium, starting at a dose of 500 micrograms once or twice daily (3). Patient responses and side effects were initially monitored subjectively by telephone every 5 to 10 days to establish the effective dose and to monitor benefits and side effects. 36 patients (90%) had reduced drooling in r ...
SINTROM®
SINTROM®

... There are many possible interactions between coumarins and other drugs. The mechanisms of these interactions include disturbances of absorption, inhibition or induction of the metabolising enzyme system (mainly CYP2C9, see section 5.2 Pharmacokinetic properties), and reduced availability of the vita ...
Biopsychosocial Model For Psychosis
Biopsychosocial Model For Psychosis

... tendency towards higher range of dose t1/2= 32 hrs, may be affected by smoking Metabolised P450 CYP1A2 & CYP2D6. No active metabolites • little effect for renal/hepatic impairment • No clinically significant interactions ...
Isomex Prolonged-release tablet ENG SmPC
Isomex Prolonged-release tablet ENG SmPC

... lactase deficiency or glucose-galactose malabsorption; should not take this medicine. Concomitant administration of Isomex and phosphodiesterase type 5 inhibitors (e.g. sildenafil, tadalafil, vardenafil) can potentiate the vasodilatory effect of Isomex with the potential result of serious side effec ...
Pharmacotheraputics
Pharmacotheraputics

... another anti-coagulant (ie. LMWH, UFH)  Note that with AFIB, you can start on warfarin alone Warfarin Genetic Testing Available: tests may be helpful in unusual patients prior to starting the drug; however, these are not widely used because it is hard to identify such patients o VKOR Deficiency: wo ...
AJWC New Drug Update 2011
AJWC New Drug Update 2011

... T cells — white blood cells that patrol the body for signs of illness. CTLA-4 serves as a control switch for the immune system’s response to disease. With no antibody attached, CTLA-4 suppresses the immune response. Ipilimumab reverses that condition, unleashing the immune attack on ...
Revised: 28th January 2009 AN: 02048/2008 SUMMARY OF
Revised: 28th January 2009 AN: 02048/2008 SUMMARY OF

... Adverse reactions (frequency and seriousness) None. ...
Pituitary Hormones
Pituitary Hormones

... - Mecasermin (recombinant human IGF-1); mecasermin rinfabate (recombinant human IGF-1 +IGF binding protein-3=IGFBP-3), given SC in dwarf with IGF-1 deficiency not responding to GH, hypoglycemia is a major side effect (less with mecasermin rinfabate) ...
Protein synthesis inhibitors Tetracyclines
Protein synthesis inhibitors Tetracyclines

... • A broad-spectrum antibiotic, is active not only against bacteria but also against other microorganisms, rickettsiae. • Chloramphenicol has excellent activity against anaerobes. ...
Antipyretic, analgesic and anti
Antipyretic, analgesic and anti

... the bark of willow & poplar tree ...
Renerve Plus Inj
Renerve Plus Inj

... In intramuscular administration, caution should be exercised by following the instructions mentioned below to avoid adverse effects on tissues or nerves. a) Avoid repeated injection at the same site. b) Do not inject in densely innervated site. c) If insertion of the injection needle causes intense ...
The Debate - HysterSisters
The Debate - HysterSisters

... or without progestins may increase your chances of getting heart attacks, strokes, breast cancer, and blood clots. Using estrogens with progestins may increase your risk of dementia (decline in memory and thinking skills). Vivelle-Dot should not be used if you have unusual vaginal bleeding; currentl ...
Benzodiazepines
Benzodiazepines

... Pharmacology of Benzodiazepines Pharmacodynamics Pharmacokinetics ...
The ideal sedative agent
The ideal sedative agent

... Pharmacology of Benzodiazepines Pharmacodynamics Pharmacokinetics ...
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Dydrogesterone



Dydrogesterone (INN, USAN, BAN), is also chemically known as 9β,10α-pregna-4,6-diene-3,20-dione. Dydrogesterone (6-dehydro-retroprogesterone) is a hormonally active, non-androgenic steroid that was developed in the 1950s.Dydrogesterone has selective progestational activity and does not inhibit ovulation. The greater rigidity of dydrogesterone also positively affects its selectivity, while natural progesterone is less selective, existing in different conformations that more easily bind to different receptors. As a consequence of its better bioavailability and the progestational activity of its main metabolites (20-, 21- and 16-hydroxy derivatives), the equivalent dose of dydrogesterone is 10–20 times lower than that of oral micronized progesterone.Dydrogesterone is used as an effective, orally active progestogen for gynaecological conditions related to a wide variety of progesterone deficiencies in pregnant women. The molecular structure and pharmacological effects are somewhat similar to endogenous progesterone, although in smaller amounts it is found to be orally active. Its freedom from hormonal effects like those related to corticoid, androgenic, estrogenic, anabolic, and other effects gives dydrogesterone an advantage over other synthesized progestogens.Dydrogesterone when used therapeutically is closely related to its physiological action on the neuro-endocrine control of ovarian function, as well as on the endometrium. This is an indication in all cases of endogeneous progesterone deficiency - relative or absolute. The molecule was licensed for use in several indications, including threatened or recurrent miscarriage, dysfunctional bleeding, infertility due to luteal insufficiency, dysmenorrhea, endometriosis, secondary amenorrhoea, irregular cycles, pre-menstrual syndrome and also as a hormone replacement therapy.Dydrogesterone has proven effective in the following conditions associated with progesterone deficiency: Infertility due to luteal insufficiency Threatened miscarriage Habitual or recurrent miscarriage. Menstrual disorders Premenstrual syndrome Endometriosis Dydrogesterone has also been registered as hormone replacement therapy (HRT) to counter-check the negative effects of unopposed estrogen on the endometrium in women with an intact uterus. Dydrogesterone is relatively safe and well tolerated, and does not exhibit the androgenic side effects that are common with some other progestins, like medroxyprogesterone acetate.
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