CREATININE powder USA - engelsk - NLM (National Library of Medicine)

creatinine powder

cbschem limited - creatinine (unii: ayi8ex34eu) (creatinine - unii:ayi8ex34eu) -

PRIFTIN- rifapentine tablet, film coated USA - engelsk - NLM (National Library of Medicine)

priftin- rifapentine tablet, film coated

sanofi-aventis u.s. llc - rifapentine (unii: xjm390a33u) (rifapentine - unii:xjm390a33u) - rifapentine 150 mg - priftin® (rifapentine) is indicated in adults and children 12 years and older for the treatment of active pulmonary tuberculosis (tb) caused by mycobacterium tuberculosis . priftin must always be used in combination with one or more antituberculosis (anti-tb) drugs to which the isolate is susceptible [see dosage and administration (2.1) and clinical studies (14.1)]. limitations of use do not use priftin monotherapy in either the initial or the continuation phases of active antituberculous treatment. priftin should not be used once weekly in the continuation phase regimen in combination with isoniazid (inh) in hiv-infected patients with active pulmonary tuberculosis because of a higher rate of failure and/or relapse with rifampin (rif)-resistant organisms [see warnings and precautions (5.4) and clinical studies (14.1)]. priftin has not been studied as part of the initial phase treatment regimen in hiv-infected patients with active pulmonary tuberculosis. priftin is indicated in adults and children 2 years an

PRIFTIN- rifapentine tablet, film coated USA - engelsk - NLM (National Library of Medicine)

priftin- rifapentine tablet, film coated

sanofi-aventis u.s. llc - rifapentine (unii: xjm390a33u) (rifapentine - unii:xjm390a33u) - rifapentine 150 mg - priftin® (rifapentine) is indicated in adults and children 12 years and older for the treatment of active pulmonary tuberculosis (tb) caused by mycobacterium tuberculosis . priftin must always be used in combination with one or more antituberculosis (anti-tb) drugs to which the isolate is susceptible [see dosage and administration (2.1) and clinical studies (14.1)] . limitations of use do not use priftin monotherapy in either the initial or the continuation phases of active antituberculous treatment. priftin should not be used once weekly in the continuation phase regimen in combination with isoniazid (inh) in hiv-infected patients with active pulmonary tuberculosis because of a higher rate of failure and/or relapse with rifampin (rif)-resistant organisms [see warnings and precautions (5.4) and clinical studies (14.1)] . priftin has not been studied as part of the initial phase treatment regimen in hiv-infected patients with active pulmonary tuberculosis. priftin is indicated in adults and children 2 years

Prolastin-C alpha1- proteinase inhibitor (human) 1000 mg powder for injection vial with diluent vial Australia - engelsk - Department of Health (Therapeutic Goods Administration)

prolastin-c alpha1- proteinase inhibitor (human) 1000 mg powder for injection vial with diluent vial

grifols australia pty ltd - alpha-1-proteinase inhibitor, quantity: 1000 mg - diluent, not applicable - excipient ingredients: - prolastin-c is an alpha-1-proteinase inhibitor (human, alpha1-pi) indicated to increase serum alpha1-pi levels in adults with congenital deficiency of alpha-1 antitrypsin and with clinically significant emphysema (fev1 less than 80%). the data for clinical efficacy of prolastin-c is derived from changes in the biomarkers alpha-1 anti-protease level and ct lung density. efficacy on fev1 or patient relevant endpoints such as quality of life or pulmonary exacerbations has not been established in randomised clinical trials. clinical trials have only included patients who were not smoking.

PROLASTIN-C (alpha-1-proteinase inhibitor- human kit
PROLASTIN-C (alpha-1-proteinase inhibitor- human kit USA - engelsk - NLM (National Library of Medicine)

prolastin-c (alpha-1-proteinase inhibitor- human kit prolastin-c (alpha-1-proteinase inhibitor- human kit

grifols usa, llc - .alpha.1-proteinase inhibitor human (unii: f43i396ois) (.alpha.1-proteinase inhibitor human - unii:f43i396ois) - .alpha.1-proteinase inhibitor human 1000 mg in 20 ml - prolastin-c is an alpha1 -proteinase inhibitor (human) (alpha1 -pi) indicated for chronic augmentation and maintenance therapy in adults with clinical evidence of emphysema due to severe hereditary deficiency of alpha1 -pi (alpha1 -antitrypsin deficiency). prolastin-c increases antigenic and functional (anti-neutrophil elastase capacity, anec) serum levels and antigenic lung epithelial lining fluid levels of alpha1 -pi. limitations of use - the effect of augmentation therapy with any alpha1 -pi, including prolastin-c, on pulmonary exacerbations and on the progression of emphysema in alpha1 -pi deficiency has not been conclusively demonstrated in randomized, controlled clinical trials. - clinical data demonstrating the long-term effects of chronic augmentation or maintenance therapy with prolastin-c are not available. - prolastin-c is not indicated as therapy for lung disease in patients in whom severe alpha1 -pi deficiency has not been established. prolastin-c is contraindicated in: - iga deficient patients w

BALVERSA 3 MG Israel - engelsk - Ministry of Health

balversa 3 mg

j-c health care ltd - erdafitinib - film coated tablets - erdafitinib 3 mg - erdafitinib - balversa is indicated for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (muc), that has:- susceptible fgfr3 or fgfr2 genetiic alterations, and- progressed during or following at least one line of prior platinum-containing chemotherapy, including within 12 months of neoadjuvant or adjuvant platinum-containing chemotherapy.

BALVERSA 4 MG Israel - engelsk - Ministry of Health

balversa 4 mg

j-c health care ltd - erdafitinib - film coated tablets - erdafitinib 4 mg - erdafitinib - balversa is indicated for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (muc), that has:- susceptible fgfr3 or fgfr2 genetiic alterations, and- progressed during or following at least one line of prior platinum-containing chemotherapy, including within 12 months of neoadjuvant or adjuvant platinum-containing chemotherapy.

BALVERSA 5 MG Israel - engelsk - Ministry of Health

balversa 5 mg

j-c health care ltd - erdafitinib - film coated tablets - erdafitinib 5 mg - erdafitinib - balversa is indicated for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (muc), that has:- susceptible fgfr3 or fgfr2 genetiic alterations, and- progressed during or following at least one line of prior platinum-containing chemotherapy, including within 12 months of neoadjuvant or adjuvant platinum-containing chemotherapy.

MINT-TRIMEBUTINE TABLET Canada - engelsk - Health Canada

mint-trimebutine tablet

mint pharmaceuticals inc - trimebutine maleate - tablet - 200mg - trimebutine maleate 200mg

MINT-TRIMEBUTINE TABLET Canada - engelsk - Health Canada

mint-trimebutine tablet

mint pharmaceuticals inc - trimebutine maleate - tablet - 100mg - trimebutine maleate 100mg