HYDROXYPROGESTERONE CAPROATE injection United States - English - NLM (National Library of Medicine)

hydroxyprogesterone caproate injection

auromedics pharma llc - hydroxyprogesterone caproate (unii: 276f2o42f5) (hydroxyprogesterone - unii:21807m87j2) - hydroxyprogesterone caproate injection is a progestin indicated to reduce the risk of preterm birth in women with a singleton pregnancy who have a history of singleton spontaneous preterm birth. the effectiveness of hydroxyprogesterone caproate injection is based on improvement in the proportion of women who delivered < 37 weeks of gestation. there are no controlled trials demonstrating a direct clinical benefit, such as improvement in neonatal mortality and morbidity. limitation of use: while there are many risk factors for preterm birth, safety and efficacy of hydroxyprogesterone caproate injection has been demonstrated only in women with a prior spontaneous singleton preterm birth. it is not intended for use in women with multiple gestations or other risk factors for preterm birth. do not use hydroxyprogesterone caproate in women with any of the following conditions: - current or history of thrombosis or thromboembolic disorders - known or suspected breast cancer, other hormone-sensitive cancer, or

HYDROXYPROGESTERONE CAPROATE injection United States - English - NLM (National Library of Medicine)

hydroxyprogesterone caproate injection

sun pharmaceutical industries, inc. - hydroxyprogesterone caproate (unii: 276f2o42f5) (hydroxyprogesterone - unii:21807m87j2) - hydroxyprogesterone caproate is a progestin indicated to reduce the risk of preterm birth in women with a singleton pregnancy who have a history of singleton spontaneous preterm birth. the effectiveness of hydroxyprogesterone caproate injection is based on improvement in the proportion of women who delivered < 37 weeks of gestation. there are no controlled trials demonstrating a direct clinical benefit, such as improvement in neonatal mortality and morbidity. limitation of use: while there are many risk factors for preterm birth, safety and efficacy of hydroxyprogesterone caproate injection has been demonstrated only in women with a prior spontaneous singleton preterm birth. it is not intended for use in women with multiple gestations or other risk factors for preterm birth. do not use hydroxyprogesterone caproate injection in women with any of the following conditions:  - current or history of thrombosis or thromboembolic disorders - known or suspected breast cancer, other hormone-sensitive cancer, or

HYDROXYPROGESTERONE CAPROATE injection United States - English - NLM (National Library of Medicine)

hydroxyprogesterone caproate injection

auromedics pharma llc - hydroxyprogesterone caproate (unii: 276f2o42f5) (hydroxyprogesterone - unii:21807m87j2) - hydroxyprogesterone caproate injection, usp is indicated in non-pregnant women: for the treatment of advanced adenocarcinoma of the uterine corpus (stage iii or iv); in the management of amenorrhea (primary and secondary) and abnormal uterine bleeding due to hormonal imbalance in the absence of organic pathology, such as submucous fibroids or uterine cancer; as a test for endogenous estrogen production and for the production of secretory endometrium and desquamation. hydroxyprogesterone caproate is contraindicated in patients with known or suspected carcinoma of the breast, other hormone-sensitive cancer, or history of these conditions; undiagnosed abnormal vaginal bleeding; liver dysfunction or disease; missed abortion, and in those with a history of hypersensitivity to the drug. hydroxyprogesterone caproate is also contraindicated as a diagnostic test for pregnancy and in patients with current or history of thrombotic or thromboembolic disorders.

HYDROXYPROGESTERONE CAPROATE injection United States - English - NLM (National Library of Medicine)

hydroxyprogesterone caproate injection

ani pharmaceuticals, inc. - hydroxyprogesterone caproate (unii: 276f2o42f5) (hydroxyprogesterone - unii:21807m87j2) - hydroxyprogesterone caproate 250 mg in 1 ml

MAKENA- hydroxyprogesterone caproate injection United States - English - NLM (National Library of Medicine)

makena- hydroxyprogesterone caproate injection

amag pharmaceuticals, inc. - hydroxyprogesterone caproate (unii: 276f2o42f5) (hydroxyprogesterone - unii:21807m87j2) - hydroxyprogesterone caproate 250 mg in 1 ml - makena is a progestin indicated to reduce the risk of preterm birth in women with a singleton pregnancy who have a history of singleton spontaneous preterm birth. the effectiveness of makena is based on improvement in the proportion of women who delivered < 37 weeks of gestation. there are no controlled trials demonstrating a direct clinical benefit, such as improvement in neonatal mortality and morbidity. limitation of use : while there are many risk factors for preterm birth, safety and efficacy of makena has been demonstrated only in women with a prior spontaneous singleton preterm birth. it is not intended for use in women with multiple gestations or other risk factors for preterm birth. do not

HYDROXY P 500 HYDROXYPROGESTERONE INJECTION Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

hydroxy p 500 hydroxyprogesterone injection

ranvet pty. limited - hydroxyprogesterone caproate - parenteral liquid/solution/suspension - hydroxyprogesterone caproate steroid-progestin active 100.0 mg/ml - endocrine system - horse mare (female) | female horse - anabolic steroid | abortion threat | androgenic properties | bone repair | catabolic complications | convalescence | erythropoietic activity | geriatric therapy | improve appetite | male sexual characterisitics | muscle development | non-virilising anabolic | pathophysiological process | protein and mineral anabolic | skeletal conditions | tissue breakdown | tissue repair | virilising anabolic

DRG Salivary 17α-Hydroxyprogesterone (17α-OHP) ELISA Singapore - English - HSA (Health Sciences Authority)

drg salivary 17α-hydroxyprogesterone (17α-ohp) elisa

biomedix singapore pte. ltd. - clinical chemistry - an enzyme immunoassay for the quantitative in vitro diagnostic measurement of active free 17 hydroxyprogesterone in saliva. measurements of 17-hydroxyprogesterone are used as an aid in the diagnosis of various disorders of the adrenal glands or the ovaries, and as an aid in the diagnosis of late onset of 21-hydroxylase deficiency, a common cause of congenital adrenal hyperplasia. this test is not intended for newborn screening.

DIAsource ImmunoAssays 17α-Hydroxyprogesterone (17-OHP)-RIA-CT Singapore - English - HSA (Health Sciences Authority)

diasource immunoassays 17α-hydroxyprogesterone (17-ohp)-ria-ct

dyamed biotech pte ltd - clinical chemistry - diasource immunoassays 17α-hydroxyprogesterone (17-ohp)-ria-ct kit is a radioimmunoassay for the in vitro quantitative measurement of human 17α-hydroxyprogesterone (17-ohp) in serum and plasma.

Lutogeston New Zealand - English - Ministry for Primary Industries

lutogeston

zoetis new zealand limited - hydroxyprogesterone caproate - hydroxyprogesterone caproate 250 g/litre - endocrine agent (hormone)