Ηνωμένες Πολιτείες - Αγγλικά - NLM (National Library of Medicine)

apotex corp. - desmopressin acetate (unii: xb13hyu18u) (desmopressin - unii:enr1llb0fp) - desmopressin acetate 0.1 mg - desmopressin acetate tablets are indicated as antidiuretic replacement therapy in the management of central diabetes insipidus and for the management of the temporary polyuria and polydipsia following head trauma or surgery in the pituitary region. desmopressin acetate is ineffective for the treatment of nephrogenic diabetes insipidus. patients were selected for therapy based on the diagnosis by means of the water deprivation test, the hypertonic saline infusion test, and/or response to antidiuretic hormone. continued response to desmopressin acetate can be monitored by measuring urine volume and osmolality. desmopressin acetate tablets are indicated for the management of primary nocturnal enuresis. desmopressin acetate may be used alone or as an adjunct to behavioral conditioning or other non-pharmacologic intervention. desmopressin acetate tablets are contraindicated in individuals with known hypersensitivity to desmopressin acetate or to any of the components of desmopressin acetate tablets. desmopressin a

Ηνωμένες Πολιτείες - Αγγλικά - NLM (National Library of Medicine)

physicians total care, inc. - megestrol acetate (unii: tj2m0fr8es) (megestrol - unii:ea6ld1m70m) - megestrol acetate 40 mg - megestrol acetate tablets are indicated for the palliative treatment of advanced carcinoma of the breast or endometrium (ie, recurrent, inoperable, or metastatic disease). it should not be used in lieu of currently accepted procedures such as surgery, radiation, or chemotherapy. history of hypersensitivity to megestrol acetate or any component of the formulation.

Αυστραλία - Αγγλικά - Department of Health (Therapeutic Goods Administration)

theramex australia pty ltd - nomegestrol acetate, quantity: 2.5 mg; estradiol hemihydrate, quantity: 1.55 mg (equivalent: estradiol, qty 1.5 mg) - tablet, film coated - excipient ingredients: crospovidone; magnesium stearate; microcrystalline cellulose; purified talc; lactose monohydrate; colloidal anhydrous silica; titanium dioxide; iron oxide yellow; polyvinyl alcohol; macrogol 3350; iron oxide black - oral contraception.

Ηνωμένες Πολιτείες - Αγγλικά - NLM (National Library of Medicine)

sandoz inc - leuprolide acetate (unii: 37jns02e7v) (leuprolide - unii:efy6w0m8tg) - leuprolide acetate 1 mg in 0.2 ml - leuprolide acetate injection is indicated in the palliative treatment of advanced prostatic cancer. leuprolide acetate injection is contraindicated in patients known to be hypersensitive to gnrh, gnrh agonist analogs or any of the excipients in leuprolide acetate injection: reports of anaphylactic reactions to gnrh agonist analogs have been reported in the medical literature. leuprolide (loo-proe-lide) acetate injection read the instructions for use before you start using leuprolide acetate injection and each time you get a refill. there may be new information. this information does not take the place of talking to your doctor about your medical condition or your treatment. your doctor should show you how to draw up leuprolide acetate injection and give the injection the right way before you inject the first time. do not share your syringes with other people, even if the needle has been changed. you may give other people a serious infection or get a serious infection from them. supplies you will need for the

Ηνωμένες Πολιτείες - Αγγλικά - NLM (National Library of Medicine)

aurobindo pharma limited - norethindrone acetate (unii: 9s44lic7oj) (norethindrone - unii:t18f433x4s) - norethindrone acetate 5 mg - norethindrone acetate tablets, usp   norethindrone acetate tablets, usp  are indicated for the treatment of secondary amenorrhea, endometriosis, and abnormal uterine bleeding due to hormonal imbalance in the absence of organic pathology, such as submucous fibroids or uterine cancer. norethindrone acetate tablets, usp  are not intended, recommended or approved to be used with concomitant estrogen therapy in postmenopausal women for endometrial protection. - known or suspected pregnancy. there is no indication for norethindrone acetate tablets in pregnancy. (see precautions .) - undiagnosed vaginal bleeding. - known, suspected or history of cancer of the breast. - active deep vein thrombosis, pulmonary embolism or history of these conditions. - active or recent (e.g., within the past year) arterial thromboembolic disease (e.g., stroke, myocardial infarction). - impaired liver function or liver disease. - as a diagnostic test for pregnancy. - hypersensitivity to any of the drug components. 

Ηνωμένες Πολιτείες - Αγγλικά - NLM (National Library of Medicine)

west-ward pharmaceutical corp - fludrocortisone acetate (unii: v47if0pvh4) (fludrocortisone - unii:u0476m545b) - fludrocortisone acetate 0.1 mg - fludrocortisone acetate tablets, 0.1 mg are indicated as partial replacement therapy for primary and secondary adrenocortical insufficiency in addison’s disease and for the treatment of salt-losing adrenogenital syndrome. corticosteroids are contraindicated in patients with systemic fungal infections and in those with a history of possible or known hypersensitivity to these agents.

Ηνωμένες Πολιτείες - Αγγλικά - NLM (National Library of Medicine)

organon usa inc. - ganirelix acetate (unii: 56u7906fqw) (ganirelix - unii:ix503l9wn0) - ganirelix acetate 250 ug in 0.5 ml - ganirelix acetate injection is indicated for the inhibition of premature lh surges in women undergoing controlled ovarian hyperstimulation. ganirelix acetate injection is contraindicated under the following conditions: - known hypersensitivity to ganirelix acetate or to any of its components including dry natural rubber/latex (see how supplied). - known hypersensitivity to gnrh or any other gnrh analog. - known or suspected pregnancy (see precautions).

Ηνωμένες Πολιτείες - Αγγλικά - NLM (National Library of Medicine)

mylan institutional llc - caspofungin acetate (unii: vuw370o5qe) (caspofungin - unii:f0xdi6zl63) - caspofungin acetate 5 mg in 1 ml - caspofungin acetate for injection is indicated as empirical therapy for presumed fungal infections in febrile, neutropenic adult and pediatric patients (3 months of age and older) [see clinical studies (14.1, 14.5)]. caspofungin acetate for injection is indicated for the treatment of candidemia and the following candida infections: intra-abdominal abscesses, peritonitis, and pleural space infections in adult and pediatric patients (3 months of age and older) [see clinical studies (14.2, 14.5)]. limitations of use: caspofungin acetate for injection has not been studied in endocarditis, osteomyelitis, and meningitis due to candida . caspofungin acetate for injection is indicated for the treatment of esophageal candidiasis in adult and pediatric patients (3 months of age and older) [see clinical studies (14.3, 14.5)]. limitations of use: caspofungin acetate for injection has not been approved for the treatment of oropharyngeal candidiasis (opc). in the study that evaluated the efficacy of caspofungin in the

Ηνωμένες Πολιτείες - Αγγλικά - NLM (National Library of Medicine)

athenex pharmaceutical division, llc. - caspofungin acetate (unii: vuw370o5qe) (caspofungin - unii:f0xdi6zl63) - caspofungin acetate 50 mg in 10.8 ml - caspofungin acetate for injection is indicated as empirical therapy for presumed fungal infections in febrile, neutropenic adult and pediatric patients (3 months of age and older) [see clinical studies ( 14.1, 14.5)]. caspofungin acetate for injection is indicated for the treatment of candidemia and the following candida infections: intra-abdominal abscesses, peritonitis, and pleural space infections in adult and pediatric patients (3 months of age and older) [see clinical studies ( 14.2, 14.5)] . limitations of use : caspofungin acetate for injection has not been studied in endocarditis, osteomyelitis, and meningitis due to candida. caspofungin acetate for injection is indicated for the treatment of esophageal candidiasis in adult and pediatric patients (3 months of age and older) [see clinical studies ( 14.3, 14.5)] . limitations of use : caspofungin acetate for injection has not been approved for the treatment of oropharyngeal candidiasis (opc). in the study that evaluated the efficacy of caspofungin in the treatment of esophageal candidiasis, patients with concomitant opc had higher relapse rate of the opc [see clinical studies ( 14.3)] . caspofungin acetate for injection is indicated for the treatment of invasive aspergillosis in adult and pediatric patients (3 months of age and older) who are refractory to or intolerant of other therapies [see clinical studies ( 14.4, 14.5)] . limitations of use : caspofungin acetate for injection has not been studied as initial therapy for invasive aspergillosis. caspofungin is contraindicated in patients with known hypersensitivity (e.g., anaphylaxis) to any component of this product [see adverse reactions ( 6)]. risk summary based on animal data, caspofungin may cause fetal harm (see data) . there are insufficient human data to establish whether there is a drug-associated risk for major birth defects, miscarriage, or adverse maternal or fetal outcomes with caspofungin use in pregnant women. in animal studies, caspofungin caused embryofetal toxicity, including increased resorptions, increased peri-implantation loss, and incomplete ossification at multiple fetal sites when administered intravenously to pregnant rats and rabbits during organogenesis at doses up to 0.8 and 2 times the clinical dose, respectively ( see data ). advise patients of the potential risk to the fetus. the estimated background risk of major birth defects and miscarriage for the indicated population is unknown. all pregnancies have a background risk of birth defect, loss, or other adverse outcomes. in the u.s. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2 to 4% and 15 to 20%, respectively. data animal data in animal reproduction studies, pregnant rats dosed intravenously with caspofungin during organogenesis (gestational days [gd] 6 to 20) at 0.5, 2, or 5 mg/kg/day (up to 0.8 times the clinical dose based on body surface area comparison) showed increased resorptions and peri-implantation losses at 5 mg/kg/day. incomplete ossification of the skull and torso and increased incidences of cervical rib were noted in offspring born to pregnant rats treated at doses up to 5 mg/kg/day. in pregnant rabbits treated with intravenous caspofungin during organogenesis (gd 7 to 20) at doses of 1, 3, or 6 mg/kg/day (approximately 2 times the clinical dose based on body surface area comparison), increased fetal resorptions and increased incidence of incomplete ossification of the talus/calcaneus in offspring were observed at the highest dose tested. caspofungin crossed the placenta in rats and rabbits and was detectable in fetal plasma. in peri- and postnatal development study in rats, intravenous caspofungin administered at 0.5, 2 or 5 mg/kg/day from day 6 of gestation through day 20 of lactation was not associated with any adverse effects on reproductive performance or subsequent development of first generation (f1) offspring or malformations in second generation (f2) offspring. risk summary there are no data on the presence of caspofungin in human milk, the effects on the breast-fed child, or the effects on milk production. caspofungin was found in the milk of lactating, drug-treated rats. the developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for caspofungin and any potential adverse effects on the breastfed child from caspofungin or from the underlying maternal condition. the safety and effectiveness of caspofungin in pediatric patients 3 months to 17 years of age are supported by evidence from adequate and well-controlled studies in adults, pharmacokinetic data in pediatric patients, and additional data from prospective studies in pediatric patients 3 months to 17 years of age for the following indications [see indications and usage ( 1)]: - empirical therapy for presumed fungal infections in febrile, neutropenic patients. - treatment of candidemia and the following candida infections: intra-abdominal abscesses, peritonitis, and pleural space infections. - treatment of esophageal candidiasis. - treatment of invasive aspergillosis in patients who are refractory to or intolerant of other therapies (e.g., amphotericin b, lipid formulations of amphotericin b, itraconazole). the efficacy and safety of caspofungin has not been adequately studied in prospective clinical trials involving neonates and infants under 3 months of age. although limited pharmacokinetic data were collected in neonates and infants below 3 months of age, these data are insufficient to establish a safe and effective dose of caspofungin in the treatment of neonatal candidiasis. invasive candidiasis in neonates has a higher rate of cns and multi-organ involvement than in older patients; the ability of caspofungin to penetrate the blood-brain barrier and to treat patients with meningitis and endocarditis is unknown. caspofungin has not been studied in pediatric patients with endocarditis, osteomyelitis, and meningitis due to candida . caspofungin has also not been studied as initial therapy for invasive aspergillosis in pediatric patients. in clinical trials, 171 pediatric patients (0 months to 17 years of age), including 18 patients who were less than 3 months of age, were given intravenous caspofungin. pharmacokinetic studies enrolled a total of 66 pediatric patients, and an additional 105 pediatric patients received caspofungin in safety and efficacy studies [see clinical pharmacology ( 12.3) and clinical studies ( 14.5)] . the majority of the pediatric patients received caspofungin at a once-daily maintenance dose of 50 mg/m 2 for a mean duration of 12 days (median 9, range 1-87 days). in all studies, safety was assessed by the investigator throughout study therapy and for 14 days following cessation of study therapy. the most common adverse reactions in pediatric patients treated with caspofungin were pyrexia (29%), blood potassium decreased (15%), diarrhea (14%), increased aspartate aminotransferase (12%), rash (12%), increased alanine aminotransferase (11%), hypotension (11%), and chills (11%) [see adverse reactions ( 6.2)]. postmarketing hepatobiliary adverse reactions have been reported in pediatric patients with serious underlying medical conditions [see warnings and precautions ( 5.3)]. clinical studies of caspofungin did not include sufficient numbers of patients aged 65 and over to determine whether they respond differently from younger patients. although the number of elderly patients was not large enough for a statistical analysis, no overall differences in safety or efficacy were observed between these and younger patients. plasma concentrations of caspofungin in healthy older men and women (65 years of age and older) were increased slightly (approximately 28% in auc) compared to young healthy men. a similar effect of age on pharmacokinetics was seen in patients with candidemia or other candida infections (intra-abdominal abscesses, peritonitis, or pleural space infections). no dose adjustment is recommended for the elderly; however, greater sensitivity of some older individuals cannot be ruled out. adult patients with mild hepatic impairment (child-pugh score 5 to 6) do not need a dosage adjustment. for adult patients with moderate hepatic impairment (child-pugh score 7 to 9), caspofungin 35 mg once daily is recommended based upon pharmacokinetic data [see clinical pharmacology ( 12.3)]. however, where recommended, a 70 mg loading dose should still be administered on day 1 [see dosage and administration ( 2.4) and clinical pharmacology ( 12.3)]. there is no clinical experience in adult patients with severe hepatic impairment (child-pugh score greater than 9) and in pediatric patients 3 months to 17 years of age with any degree of hepatic impairment. no dosage adjustment is necessary for patients with renal impairment. caspofungin is not dialyzable; thus, supplementary dosing is not required following hemodialysis [see clinical pharmacology ( 12.3)].

Ηνωμένες Πολιτείες - Αγγλικά - NLM (National Library of Medicine)

fresenius kabi usa, llc - caspofungin acetate (unii: vuw370o5qe) (caspofungin - unii:f0xdi6zl63) - caspofungin acetate 5 mg in 1 ml - caspofungin acetate for injection is indicated as empirical therapy for presumed fungal infections in febrile, neutropenic adult and pediatric patients (3 months of age and older) [see clinical studies (14.1,14.5)] . caspofungin acetate for injection is indicated for the treatment of candidemia and the following candida infections: intra-abdominal abscesses, peritonitis, and pleural space infections in adult and pediatric patients (3 months of age and older) [see clinical studies (14.2, 14.5)] . limitations of use: caspofungin acetate for injection has not been studied in endocarditis, osteomyelitis, and meningitis due to candida . caspofungin acetate for injection is indicated for the treatment of esophageal candidiasis in adult and pediatric patients (3 months of age and older) [see clinical studies (14.3, 14.5)]. limitations of use: caspofungin acetate for injection has not been approved for the treatment of oropharyngeal candidiasis (opc). in the study that evaluated the efficacy of caspofungin in the