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Opioid-Induced Constipation - American College of Gastroenterology
Opioid-Induced Constipation - American College of Gastroenterology

... gastrointestinal recovery following partial large or small bowel resection surgery with primary anastomosis; it is available only for short-term (15 doses) use in hospitalized patients, and it can only be prescribed in hospitals that have registered in and met all of the requirements for the ENTEREG ...
Veterinary Antibiotics
Veterinary Antibiotics

... Adverse effects: Hypersensitivity, GI, CNS stimulation, crystaluria Contraindications: hypersensitivity, relative CI in young growing animals due to cartilage abnormalities Caution: hepatic or renal insufficiency, dehydration Administration: PO preferably on an empty stomach Interactions: Antacids, ...
Product Information for Triptorelin Acetate
Product Information for Triptorelin Acetate

... Excessive ovarian response to gonadotrophin treatment seldom gives rise to OHSS unless hCG is administered to trigger ovulation. Therefore in cases of OHSS it is prudent to withhold hCG and advise the patient to refrain from coitus or to use barrier methods for at least 4 days. OHSS may progress rap ...
Memorandum
Memorandum

... were able to be marketed as a dietary supplement. We have significant concerns about the evidence on which you rely to support your conclusion that a dietary supplement containing AHYP will reasonably be expected to be safe. Your submission indicates that use of AHYP may result in adverse effects. Y ...
ATROVENT® Metered Aerosol (CFC-free) - Boehringer
ATROVENT® Metered Aerosol (CFC-free) - Boehringer

... L (approximately 4.6 L/kg). The half-life of the terminal elimination phase is about 1.6 hours. The drug is less than 20% bound to plasma proteins. The ipratropium ion does not cross the blood-brain barrier, consistent with the ammonium structure of the molecule. Metabolism The mean total clearance ...
Rapid Reversal of Anticoagulation in Trauma Patients
Rapid Reversal of Anticoagulation in Trauma Patients

... • Vitamin K - Oral administration results in correction by 24 hours. - IV administration is marginally faster (small risk of anaphylaxis). ...
Ontwikkeling en validatie van een hoge druk
Ontwikkeling en validatie van een hoge druk

... Broad spectrum of activity (yeasts and moulds) Rapidly and highly fungicidal, stable to resistance Potent in vivo activity (even in neutropenia) ...
BAHAGIAN PERKHIDMATAN FARMASI
BAHAGIAN PERKHIDMATAN FARMASI

... valganciclovir and that of aciclovir and valaciclovir, a cross-hypersensitivity reaction between these drugs is possible. Interaction Drug interaction studies with valganciclovir have not been performed, but since it undergoes rapid conversion to ganciclovir, interactions are likely to be the same a ...
Anticoagulants - Faculty Sites
Anticoagulants - Faculty Sites

... Objective 4: list the appropriate routes to administer heparin ...
STRUCTURAL ACTIVITY RELATIONSHIP AMONG THE
STRUCTURAL ACTIVITY RELATIONSHIP AMONG THE

... cholinergic) activity; for maximum potency, the size of the alkyl groups substituted on the nitrogen should not exceed the size of a methyl group; ...
Opioid analgesics in palliative care
Opioid analgesics in palliative care

... inhibitors (eg, paroxetine, haloperidol and levomepromazine) may also derive reduced benefit from codeine. Codeine is considered one 10th as potent as morphine. As a general rule, products containing less than 30mg of codeine per dose are not suitable step 2 analgesics. Despite being a weak opioid, ...
CHILD RESISTANT PACKAGING REGULATION
CHILD RESISTANT PACKAGING REGULATION

... oral drugs packed in unit dose packs: any child of 11.4 kg* who opens or gains access to the number of individual units which constitute the “harmful dose”, or a child who opens or gains access to more than 8 individual units  The CFR title 16, part 1700 discusses packaging test procedures extensiv ...
Analgesics antipyretics nonsteroidal anti inflammatory
Analgesics antipyretics nonsteroidal anti inflammatory

... NSAIDs (nonsteroidal anti-inflammatory drugs) NSAIDs, including ibuprofen , have analgesic, anti-inflammatory and antipyretic properties. In single doses NSAIDs have analgesic activity comparable to that of paracetamol. In regular full dosage, they have a lasting analgesic and antiinflammatory effec ...
Analgesics, antipyretics, nonsteroidal anti
Analgesics, antipyretics, nonsteroidal anti

... NSAIDs (nonsteroidal anti-inflammatory drugs) NSAIDs, including ibuprofen , have analgesic, anti-inflammatory and antipyretic properties. In single doses NSAIDs have analgesic activity comparable to that of paracetamol. In regular full dosage, they have a lasting analgesic and antiinflammatory effec ...


... not differ significantly between the two groups. The incidence of side effects was higher after the 400 mg dose. As it is known that clinically significant retinopathy has not been found after a daily dose of 200 mg hydroxychloroquine the effectiveness of this dose is of practical importance. After ...
Screening of Wrightia tinctoria leaves for Anti psoriatic activity (PDF
Screening of Wrightia tinctoria leaves for Anti psoriatic activity (PDF

... Plan: The hydro alcoholic extract of Wrightia tinctoria leaves was evaluated for antipsoriatic activity by mouse tail test. Methodology: Antipsoriatic activity was performed at a dose 200 mg/kg body weight in mice (25-30 g). Isoretinoic acid (0.5 mg/kg) was used as the standard. Degree of orthokerat ...
HIGHLIGHTS OF PRESCRIBING INFORMATION Clostridium difficile
HIGHLIGHTS OF PRESCRIBING INFORMATION Clostridium difficile

... osteoporosis-related fractures of the hip, wrist or spine. The risk of fracture was increased in patients who received high-dose, defined as multiple daily doses, and long-term PPI therapy (a year or longer). Patients should use the lowest dose and shortest duration of PPI therapy appropriate to the ...
HYDROCHLOROTHIAZIDE TABLETS USP 25 mg and 50
HYDROCHLOROTHIAZIDE TABLETS USP 25 mg and 50

... Teratogenic Effects - Pregnancy Category B Studies in which hydrochlorothiazide was orally administered to pregnant mice and rats during their respective periods of major organogenesis at doses up to 3000 and 1000 mg hydrochlorothiazide/kg, respectively, provided no evidence of harm to the fetus. Th ...
Pregabalin (Lyrica™) - A new treatment option for neuropathic pain
Pregabalin (Lyrica™) - A new treatment option for neuropathic pain

... food or on an empty stomach. Based on response and tolerability, the dosage may be increased to 150 mg twice daily after an interval of 3 to 7 days.3 If treatment is to be discontinued, it is recommended that this should be done gradually over at least one week. ...
Dabigatran
Dabigatran

... recently stopped because [dabigatran] users were more likely to experience strokes, heart attacks, and blood clots forming on the mechanical heart valves than were users of the anticoagulant warfarin. There was also more bleeding after valve surgery in the [dabigatran] users than in the warfarin use ...
Number: PL 00006/0195
Number: PL 00006/0195

... thoughts, self harm and suicide (suicide-related events). This risk persists until significant remission occurs. As improvement may not occur during the first few weeks or more of treatment, patients should be closely monitored until such improvement occurs. It is general clinical experience that th ...
Clinical Insights: Opioid-sparing Pain Management in Oral
Clinical Insights: Opioid-sparing Pain Management in Oral

... 1. Data on file. Pacira Pharmaceuticals, Inc. Parsippany, NJ. 2. Walawender I, Roczniak W, Nowak D, et al. Applicability of the numeric scale for anxiety evaluation in patients undergoing dental treatment. Dent Med Probl. 2015;52(2):205214. 3. van Wijk AJ, Makkes PC. Highly anxious dental patients r ...
Guidelines for Use of Meperidine
Guidelines for Use of Meperidine

... Problems associated with meperidine use have resulted in inadequate pain control and adverse effects for many patients through the years. First-line opioids such as morphine, hydromorphone or oxycodone should be used in preference to meperidine, which should be utilized only as outlined below. Meper ...
IOSR Journal of Dental and Medical Sciences (IOSR-JDMS)
IOSR Journal of Dental and Medical Sciences (IOSR-JDMS)

... arachidonic acid metabolism. Following administration of single doses, the pharmacokinetics of piroxicam is linear. Maximum plasma concentrations are usually attained in about 2 hours, but may vary between 1 and 6 hours in different subjects. Piroxicam is eliminated largely by biotransformation, the ...
Ref: Choudhury et al
Ref: Choudhury et al

... • Highly significant reduction in Bilirubin, Alkaline phosphatase, SGOT, SGPT. • Highly significant increase in Serum protein and Albumin Globulin ratio ...
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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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