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Sulodexide - Wiley Online Library
Sulodexide - Wiley Online Library

... observed in the kidney, liver and endothelium of veins and arteries (21,67). The pharmacokinetics in man has been evaluated using deuterium-labeled sulodexide (12). A single 100 mg dose of deuterated sulodexide was administered to healthy volunteers intravenously or orally. After intravenous dosage ...
Anti-nociceptive activity of ethylacetate fraction of
Anti-nociceptive activity of ethylacetate fraction of

... Administration of EAFCF orally at the doses of 50,100, and 200 mg/kg dose dependently reduced the paw licking induced by formalin in both early and late phases of the experiment (p<0.001). A complete inhibition of licking in late phase was evident from morphine treated animals (Table 4). 3.6. Effect ...
The Haunting of Medical Journals: How Ghostwriting Sold ``HRT``
The Haunting of Medical Journals: How Ghostwriting Sold ``HRT``

... Dozens of ghostwritten reviews and commentaries published in medical journals and supplements were used to promote unproven benefits and downplay harms of menopausal hormone therapy (HT), and to cast raloxifene and other competing therapies in a negative light. Specifically, the pharmaceutical compa ...
Full Product Information
Full Product Information

... In addition to its anti-H1 effect, cetirizine was shown to display anti-allergic activities: at a dose of 10 mg once or twice daily, it inhibits the late phase recruitment of inflammatory cells, notably eosinophils, in the skin and conjunctiva of atopic subjects submitted to antigen challenge, and t ...
gastrointestinal agents - Magellan Health Services || TennCare Portal
gastrointestinal agents - Magellan Health Services || TennCare Portal

... doses (2mg) of buprenorphine μ-opioid receptor occupancy is approximately 41%, and then for 8, 16, and 32mg the occupancy increases to 83%, 92%, and 98%. Additionally, the study results also demonstrated that receptor availability did not change significantly between between 16mg and 32mg but doses ...
β-Blocker Ingestion: An Evidence-Based Consensus
β-Blocker Ingestion: An Evidence-Based Consensus

... with stated or suspected self-harm or who are the victims of a potentially malicious administration of b-blocker should be referred to an emergency department immediately. In general, this should occur regardless of the dose reported (Grade D). 2) Patients without evidence of self-harm should have f ...
Prescribing Information
Prescribing Information

... these reasons, in patients undergoing elective surgery, some authorities recommend gradual withdrawal of betaadrenergic receptor blocking agents. If necessary during surgery, the effects of beta-adrenergic blocking agents may be reversed by sufficient doses of adrenergic agonists. ...
Cephalosporins and Related Antibiotics Therapeutic Class Review (TCR) January 7, 2014
Cephalosporins and Related Antibiotics Therapeutic Class Review (TCR) January 7, 2014

... * Cephalexin is additionally indicated for bone infections, acute prostatitis and respiratory tract infections, both upper and lower, due to susceptible organisms. ** Amoxicillin/clavulanate (Augmentin) tablets are additionally indicated for lower respiratory tract infections due to susceptible orga ...
C11 Chemistry 151 Whitesell The Provisional Progress of
C11 Chemistry 151 Whitesell The Provisional Progress of

... had harmful side effects when taken in large doses. Therefore, prednisone was utilized as a corticosteroid in high doses at a short period of time, in order to decrease the risks of dangerous side effects. The FDA first approved prednisone in 1955. It is prescribed to Duchenne Muscular Dystrophy pat ...
caelyx - Janssen
caelyx - Janssen

... Growth factor support was required infrequently (<5%) and transfusion support was required in approximately 15% of patients. Because of this potential for bone marrow suppression, careful hematologic monitoring is required during use of CAELYX®. Complete blood counts, including platelet counts, shou ...
Neurogenic temporomandibular joint dislocation treated with
Neurogenic temporomandibular joint dislocation treated with

... accident, he presented multiple foci of brain contusions, with subarachnoid bleeding in the third and lateral ventricles, the right thalamus, and the right occipital cortex. These injuries led to the presence of chronic subdural haematomas. He also suffered diaphyseal fracture of the right humerus, ...
FABRICATION, EVALUATION AND PRELIMINARY CLINICAL STUDY OF BI-LAYER OROBUCCAL
FABRICATION, EVALUATION AND PRELIMINARY CLINICAL STUDY OF BI-LAYER OROBUCCAL

... include changes in the morphology of gingival tissue such as oedema, redness, reduction in consistence, and bleeding upon probing as well as loss of attachment and periodontal pocket formation. Periodontal pocket provides an ideal environment for the growth and proliferation of anaerobic pathogenic ...
Potency of Kara sooda sathu parpam, a herbo mineral siddha drug
Potency of Kara sooda sathu parpam, a herbo mineral siddha drug

... Siddha is one of the Indian systems of medicine which is widely practised in Tamil Nadu, India. Siddha insists to lead a healthy life both physically and mentally by keeping pace with the laws of nature. Siddhas have classified 4448 diseases, based on the three humoral pathologies. Among them Kallad ...
Dabigatran
Dabigatran

... • No significant difference in the rate of major bleeding for dabigatran 150 mg BID compared to warfarin – 3.11 vs 3.36 %/yr; p=0.31 • Rate of major bleeding with dabigatran 110 mg BID (2.71%/yr) was 20% lower compared to warfarin; p=0.003 ...
Endocrine disrupting substances
Endocrine disrupting substances

... that are released into the environment, with special emphasis on Swedish conditions. Following the evaluation of existing knowledge, recommendations for future research are given. In the present report we are primarily focusing on chemicals that have the potential of interfering, as agonists or anta ...
evaluation of ethanolic leaf extract of dioscorea hispida dennst
evaluation of ethanolic leaf extract of dioscorea hispida dennst

... acetic acid induced writhing methods to assess its analgesic activity. The extract was also evaluated for its antiinflammatory activity by subjecting it to ‘carrageenan’ induced paw oedema test for its effect on acute phase inflammation models in rats, as well as analgesic activity in mice. It was f ...
Comparison of High Loading Dose Versus Usual Dose of Rectal
Comparison of High Loading Dose Versus Usual Dose of Rectal

... patients administered a high dose rectal acetaminophen comparing to the patients treated with a low dose acetaminophen. After one hour, the frequency of patients who showed a 2°C decrease in their body temperature was not different in the two groups but this difference was significant three hours af ...
Cataflam® Voltaren® Voltaren
Cataflam® Voltaren® Voltaren

... Under fasting condition, diclofenac is completely absorbed from the gastrointestinal tract. However, due to first-pass metabolism, only about 50% of the absorbed dose is systemically available. Cataflam Immediate-Release Tablets: In some fasting volunteers, measurable plasma levels are observed with ...
Flagyl Prescribing Information
Flagyl Prescribing Information

... fertility: Metronidazole has shown evidence of carcinogenic activity in a number of studies involving chronic, oral administration in mice and rats. Prominent among the effects in the mouse was the promotion of pulmonary tumorigenesis. This has been observed in all six reported studies in that speci ...
Ketamine - Medicines Management
Ketamine - Medicines Management

... is due to non-competitive antagonism of the NMDA receptor. Ketamine interacts with specific binding site on the NMDA receptor, blocking the influx of Na and Ca. Binding of ketamine will only occur when the ion channel has been opened though neuronal excitation. The analgesic activity is believed to ...
PACKAGE INSERT TEMPLATE FOR LOPERAMIDE
PACKAGE INSERT TEMPLATE FOR LOPERAMIDE

... Loperamide undergoes significant first pass metabolism in the liver. Oxidative N-demethylation is the main metabolic pathway for loperamide, and is mediated mainly through CYP3A4 and CYP2C8. Oxidative ndealkylation may be another pathway. Due to this very high first pass effect; plasma concentration ...
Emtriva - Gilead Sciences, Inc.
Emtriva - Gilead Sciences, Inc.

... EMTRIVA is a component of ATRIPLA (a fixed-dose combination of efavirenz, emtricitabine, and tenofovir disoproxil fumarate), COMPLERA (a fixed-dose combination of emtricitabine, rilpivirine, and tenofovir disoproxil fumarate), STRIBILD (a fixed-dose combination of elvitegravir, cobicistat, emtricita ...
1-28-17 PPT
1-28-17 PPT

... Which of the following is not true of the adverse effects of chloroquine? a. Visual impairment is related the affinity of chloroquine for melanin areas in the eye b. Low blood levels due to distribution to tissues increases the toxicity of chloroquine c. Ototoxicity, myopathy, and peripheral neurop ...
combination oral contraceptive pill
combination oral contraceptive pill

... appear to be more potent than the estrane derivatives (smaller doses can be used), but otherwise differences between the estrane and gonane compounds are difficult to characterize. ...
Welcome to AROMASIN Continuing your treatment journey
Welcome to AROMASIN Continuing your treatment journey

... in postmenopausal women, but has no detectable effect on adrenal biosynthesis of corticosteroids or aldosterone. Exemestane has no effect on other enzymes involved in the steroidogenic pathway up to a concentration at least 600 times higher than that inhibiting the aromatase enzyme. 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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