BICALUTAMIDE HIKMA 50 Milligram Film Coated Tablet Ireland - English - HPRA (Health Products Regulatory Authority)

bicalutamide hikma 50 milligram film coated tablet

hikma farmaceutica (portugal) sa - bicalutamide - film coated tablet - 50 milligram - anti-androgens

Voriconazole Hikma (previously Voriconazole Hospira) European Union - English - EMA (European Medicines Agency)

voriconazole hikma (previously voriconazole hospira)

hikma farmaceutica (portugal) s.a. - voriconazole - bacterial infections and mycoses; aspergillosis; candidiasis - antimycotics for systemic use - voriconazole is a broad spectrum, triazole antifungal agent and is indicated in adults and children aged 2 years and above as follows:treatment of invasive aspergillosis;treatment of candidaemia in non-neutropenic patients;treatment of fluconazole-resistant serious invasive candida infections (including c. krusei);treatment of serious fungal infections caused by scedosporium spp. and fusarium spp.voriconazole should be administered primarily to patients with progressive, possibly life-threatening infections.prophylaxis of invasive fungal infections in high risk allogeneic hematopoietic stem cell transplant (hsct)recipients.

Caspofungin Hikma 50 mg powder for concentrate for solution for infusion Malta - English - Medicines Authority

caspofungin hikma 50 mg powder for concentrate for solution for infusion

hikma farmacêutica (portugal),sa estrada do rio da mó, 8, 8a e 8b, fervença, terrugem, snt, 2705-906, portugal - caspofungin acetate - powder for concentrate for solution for infusion - caspofungin acetate 50 mg - antimycotics for systemic use

Caspofungin Hikma 70 mg powder for concentrate for solution for infusion Malta - English - Medicines Authority

caspofungin hikma 70 mg powder for concentrate for solution for infusion

hikma farmacêutica (portugal),sa estrada do rio da mó, 8, 8a e 8b, fervença, terrugem, snt, 2705-906, portugal - caspofungin acetate - powder for concentrate for solution for infusion - caspofungin acetate 70 mg - antimycotics for systemic use

Teicoplanin Hikma 200mg Powder for solution for injection/infusion or oral solution Ireland - English - HPRA (Health Products Regulatory Authority)

teicoplanin hikma 200mg powder for solution for injection/infusion or oral solution

hikma farmacêutica (portugal) s.a. - teicoplanin - powder for solution for injection/infusion - 200 milligram(s) - glycopeptide antibacterials; teicoplanin

Teicoplanin Hikma 400mg Powder for solution for injection/infusion or oral solution Ireland - English - HPRA (Health Products Regulatory Authority)

teicoplanin hikma 400mg powder for solution for injection/infusion or oral solution

hikma farmacêutica (portugal) s.a. - teicoplanin - powder for solution for injection/infusion - 400 milligram(s) - glycopeptide antibacterials; teicoplanin

LEVOFLOXACIN injection, solution United States - English - NLM (National Library of Medicine)

levofloxacin injection, solution

hikma pharmaceuticals usa inc. - levofloxacin (unii: 6gnt3y5lmf) (levofloxacin anhydrous - unii:rix4e89y14) - levofloxacin anhydrous 250 mg in 50 ml - levofloxacin injection is indicated for the treatment of adults (≥ 18 years of age) with mild, moderate, and severe infections caused by susceptible isolates of the designated microorganisms in the conditions listed in this section. levofloxacin injection is indicated when intravenous administration offers a route of administration advantageous to the patient (e.g., patient cannot tolerate an oral dosage form). levofloxacin is indicated for the treatment of nosocomial pneumonia due to methicillin-susceptible staphylococcus aureus , pseudomonas aeruginosa , serratia marcescens , escherichia coli , klebsiella pneumoniae , haemophilus influenzae , or streptococcus pneumoniae . adjunctive therapy should be used as clinically indicated. where pseudomonas aeruginosa is a documented or presumptive pathogen, combination therapy with an anti-pseudomonal β-lactam is recommended [see clinical studies (14.1) ]. levofloxacin is indicated for the treatment of community-acquired pneumonia due to methicillin-susceptible sta

LEVOFLOXACIN injection, solution United States - English - NLM (National Library of Medicine)

levofloxacin injection, solution

hikma pharmaceuticals usa inc. - levofloxacin (unii: 6gnt3y5lmf) (levofloxacin anhydrous - unii:rix4e89y14) - levofloxacin injection is indicated for the treatment of adults (≥ 18 years of age) with mild, moderate, and severe infections caused by susceptible isolates of the designated microorganisms in the conditions listed in this section. levofloxacin injection is indicated when intravenous administration offers a route of administration advantageous to the patient (e.g., patient cannot tolerate an oral dosage form). levofloxacin is indicated for the treatment of nosocomial pneumonia due to methicillin-susceptible staphylococcus aureus , pseudomonas aeruginosa , serratia marcescens , escherichia coli , klebsiella pneumoniae , haemophilus influenzae , or streptococcus pneumoniae . adjunctive therapy should be used as clinically indicated. where pseudomonas aeruginosa is a documented or presumptive pathogen, combination therapy with an anti-pseudomonal β-lactam is recommended [see clinical studies (14.1) ]. levofloxacin is indicated for the treatment of community-acquired pneumonia due to methicillin-susceptible sta