Optaflu Europeiska unionen - engelska - EMA (European Medicines Agency)

optaflu

seqirus gmbh - influenza virus surface antigens (haemagglutinin and neuraminidase), inactivated, of the following strains:a/california/7/2009 (h1n1)pdm09 - like strain(a/brisbane/10/2010, wild type)a/switzerland/9715293/2013 (h3n2) - like strain(a/south australia/55/2014, wild type)b/phuket/3073/2013–like strain(b/utah/9/2014, wild type) - influenza, human; immunization - vaccines - prophylaxis of influenza for adults, especially in those who run an increased risk of associated complications.optaflu should be used in accordance to official guidance.

Cardiopulmonary bypass system centrifugal pump Australien - engelska - Department of Health (Therapeutic Goods Administration)

cardiopulmonary bypass system centrifugal pump

lovell surgical supplies international pty ltd - 31718 - cardiopulmonary bypass system centrifugal pump - the deltastream blood pump is intended for pumping human blood or similar liquids while connected to extracorporeal circuits. it can be used for neonatal, pediatric and adult patients as well as for isolated organs. the usual application of the pump is pulmonary, circulatory or combined cardio-pulmonary support in combination with components of a cardiopulmonary bypass system as commonly used in clinical settings and complying with clinical standards. the period of application is limited to 7 days. the deltastream dp3 pump head must be exclusively used in combination with the deltastream mdc consoles, dc or bdc, the deltastream mdc dp3 or dc dp3 drive units, and related accessories. furthermore, the dp3 pump head can be operated with the ila activve, i-cor console and xenios console and related accessories.

SOLU-MEDROL- methylprednisolone sodium succinate injection, powder, for solution USA - engelska - NLM (National Library of Medicine)

solu-medrol- methylprednisolone sodium succinate injection, powder, for solution

general injectables & vaccines, inc - methylprednisolone sodium succinate (unii: lec9gky20k) (methylprednisolone - unii:x4w7zr7023) - methylprednisolone 40 mg in 1 ml - when oral therapy is not feasible, and the strength, dosage form, and route of administration of the drug reasonably lend the preparation to the treatment of the condition, the intravenous or intramuscular use of solu-medrol sterile powder is indicated as follows: allergic states: control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, serum sickness, transfusion reactions. dermatologic diseases: bullous dermatitis herpetiformis, exfoliiative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (stevens-johnson syndrome). endocrine disorders: primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy, mineralocorticoid supplementation is of particular importance), congenital

Flucelvax Tetra Europeiska unionen - engelska - EMA (European Medicines Agency)

flucelvax tetra

seqirus netherlands b.v. - a/darwin/6/2021(h3n2)-like strain (a/darwin/11/2021, wild type) / a/wisconsin/67/2022 (h1n1)pdm09-like strain (a/georgia/12/2022 cvr-167) / b/austria/1359417/2021-like strain (b/singapore/wuh4618/2021) / b/phuket/3073/2013-like virus (b/singapore/inftt-16-0610/2016, wild type) - influenza, human - influenza, inactivated, split virus or surface antigen - prophylaxis of influenza in adults and children from 2 years of age.flucelvax tetra should be used in accordance with official recommendations.

SOLU-MEDROL- methylprednisolone sodium succinate injection, powder, for solution USA - engelska - NLM (National Library of Medicine)

solu-medrol- methylprednisolone sodium succinate injection, powder, for solution

general injectables & vaccines, inc - methylprednisolone sodium succinate (unii: lec9gky20k) (methylprednisolone - unii:x4w7zr7023) - when oral therapy is not feasible, and the strength, dosage form, and route of administration of the drug reasonably lend the preparation to the treatment of the condition, the intravenous or intramuscular use of solu-medrol sterile powder is indicated as follows: allergic states : control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, serum sickness, transfusion reactions. dermatologic diseases : bullous dermatitis herpetiformis, exfoliiative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (stevens-johnson syndrome). endocrine disorders: primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy, mineralocorticoid supplementation is of particular importance), congeni

DUODART Israel - engelska - Ministry of Health

duodart

glaxo smith kline (israel) ltd - dutasteride; tamsulosin hydrochloride - capsules - dutasteride 0.5 mg; tamsulosin hydrochloride 0.4 mg - tamsulosin - treatment of moderate to severe symptoms of benign prostatic hyperplasia (bph). reduction in the risk of acute urinary retention (aur) and surgery in patients with moderate to severe symptoms of bph.

DUODART Israel - engelska - Ministry of Health

duodart

glaxo smith kline (israel) ltd - dutasteride; tamsulosin hydrochloride - capsules - dutasteride 0.5 mg; tamsulosin hydrochloride 0.4 mg - tamsulosin - treatment of moderate to severe symptoms of benign prostatic hyperplasia (bph). reduction in the risk of acute urinary retention (aur) and surgery in patients with moderate to severe symptoms of bph.

DUODART Israel - engelska - Ministry of Health

duodart

glaxo smith kline (israel) ltd - dutasteride; tamsulosin hydrochloride - capsules - dutasteride 0.5 mg; tamsulosin hydrochloride 0.4 mg - tamsulosin - treatment of moderate to severe symptoms of benign prostatic hyperplasia (bph). reduction in the risk of acute urinary retention (aur) and surgery in patients with moderate to severe symptoms of bph.

SOLU-MEDROL- methylprednisolone sodium succinate injection, powder, for solution USA - engelska - NLM (National Library of Medicine)

solu-medrol- methylprednisolone sodium succinate injection, powder, for solution

henry schein, inc. - methylprednisolone sodium succinate (unii: lec9gky20k) (methylprednisolone - unii:x4w7zr7023) - when oral therapy is not feasible, and the strength, dosage form, and route of administration of the drug reasonably lend the preparation to the treatment of the condition, the intravenous or intramuscular use of solu-medrol sterile powder is indicated as follows: allergic states: control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, serum sickness, transfusion reactions. dermatologic diseases: bullous dermatitis herpetiformis, exfoliiative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (stevens-johnson syndrome). endocrine disorders: primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy, mineralocorticoid supplementation is of particular importance), congenital