MITOMYCIN ACCORD mitomycin powder for injection 2mg vial Australia - inglese - Department of Health (Therapeutic Goods Administration)

mitomycin accord mitomycin powder for injection 2mg vial

omegapharm - mitomycin, quantity: 2 mg - injection, powder for - excipient ingredients: mannitol - mitomycin is indicated in the palliative treatment of carcinoma of the stomach, pancreas, colon, lung (non-small cell), breast, cervix, head and neck, liver and bladder.

DEXMEDETOMIDINE HYDROCHLORIDE INJECTION SOLUTION Canada - inglese - Health Canada

dexmedetomidine hydrochloride injection solution

omega laboratories limited - dexmedetomidine (dexmedetomidine hydrochloride) - solution - 200mcg - dexmedetomidine (dexmedetomidine hydrochloride) 200mcg

DEXMEDETOMIDINE HYDROCHLORIDE INJECTION SOLUTION Canada - inglese - Health Canada

dexmedetomidine hydrochloride injection solution

omega laboratories limited - dexmedetomidine (dexmedetomidine hydrochloride) - solution - 400mcg - dexmedetomidine (dexmedetomidine hydrochloride) 400mcg

ERYTHROMYCIN PANPHARMA erythromycin (as lactobionate) 1 g powder for Injection vial Australia - inglese - Department of Health (Therapeutic Goods Administration)

erythromycin panpharma erythromycin (as lactobionate) 1 g powder for injection vial

panpharma australia pty ltd - erythromycin lactobionate, quantity: 1.49 g (equivalent: erythromycin, qty 1 g) - injection, powder for - excipient ingredients: - oral erythromycin is not considered to be the antibiotic of choice in severely ill patients.,erythromycin panpharma (sterile erythromycin lactobionate) is indicated in the treatment of infections caused by susceptible strains of the designated organisms in the diseases listed below when oral administration is not possible or when the severity of the infection requires immediate high serum levels of erythromycin. intravenous therapy should be replaced by oral administration at the appropriate time.,? upper respiratory tract infections caused by streptococcus pyogenes (group a beta-haemolytic streptococci); streptococcus pneumoniae (diplococcus pneumoniae); haemophilus influenzae (many strains of h. influenzae are not susceptible to the erythromycin concentrations ordinarily achieved).,? lower respiratory tract infections caused by streptococcus pyogenes (group a beta-haemolytic streptococci); streptococcus pneumoniae (diplococcus pneumoniae).,? respiratory tract infections due to mycoplasma pneumoniae.,? skin and skin structure infections caused by streptococcus pyogenes and staphylococcus aureus (resistant staphylococci may emerge during treatment).,? diphtheria - as an adjunct to diphtheria antitoxin in infections due to corynebacterium diphtheriae to prevent establishment of carriers and to eradicate the organism in carriers.,? acute pelvic inflammatory disease caused by neisseria gonorrhoeae: erythromycin panpharma (sterile erythromycin lactobionate) followed by erythromycin stearate, base or ethyl succinate orally, as an alternative drug in treatment of acute pelvic inflammatory disease caused by n. gonorrhoeae in female patients with a history of sensitivity to penicillin.,? before treatment of gonorrhoea, patients who are suspected of also having syphilis should have microscopic examination for t. pallidum (by immuno-fluorescence or dark field) before receiving erythromycin and monthly serologic tests for a minimum of 4 months thereafter.,? legionnaires' disease caused by legionella pneumophila. although no controlled clinical efficacy studies have been conducted, in vitro and limited preliminary clinical data suggest that erythromycin may be effective in treating legionnaires' disease.

HYDROCORTISONE PANPHARMA hydrocortisone sodium succinate 100 mg powder for injection vial Australia - inglese - Department of Health (Therapeutic Goods Administration)

hydrocortisone panpharma hydrocortisone sodium succinate 100 mg powder for injection vial

panpharma australia pty ltd - hydrocortisone sodium succinate, quantity: 133.7 mg - injection, powder for - excipient ingredients: dibasic sodium phosphate; monobasic sodium phosphate - when oral therapy is not feasible, and the strength, form and route of administration of the drug reasonably lend the preparation to the treatment of the condition, hydrocortisone panpharma powder for injection is indicated for intravenous or intramuscular use in the following conditions:,1. endocrine disorders ? primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogues may be used in conjunction with mineralocorticoids where applicable; in infancy, mineralocorticoid supplementation is of particular importance). acute adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; mineralocorticoid supplements may be necessary, particularly when synthetic analogues are used). ? preoperatively and in the event of serious trauma or illness, in patients with known adrenal insufficiency or when adrenocortical reserve is doubtful ? shock unresponsive to conventional therapy if adrenocortical insufficiency exists or is suspected ? congenital adrenal hyperplasia ? nonsuppurative thyroiditis ? hypercalcaemia associated with cancer. 2. rheumatic disorders as adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in: ? post-traumatic osteoarthritis ? synovitis of osteoarthritis ? rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy) ? acute and subacute bursitis ? epicondylitis ? acute nonspecific tenosynovitis ? acute gouty arthritis ? psoriatic arthritis ? ankylosing spondylitis.,3. collagen diseases during an exacerbation or as maintenance therapy in selected cases of: ? systemic lupus erythematosus ? systemic dermatomyositis (polymyositis) ? acute rheumatic carditis.,4. dermatological diseases ? pemphigus ? severe erythema multiforme (stevens-johnson syndrome) ? exfoliative dermatitis ? bullous dermatitis herpetiformis ? severe seborrhoeic dermatitis ? severe psoriasis ? mycosis fungoides.,5. allergic states control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in: ? bronchial asthma ? drug hypersensitivity reactions ? contact dermatitis ? urticarial transfusion reactions ? atopic dermatitis ? serum sickness ? seasonal or perennial allergic rhinitis ? acute noninfectious laryngeal oedema (adrenaline is the drug of first choice).,6. ophthalmic diseases severe acute and chronic allergic and inflammatory processes involving the eye, such as: ? herpes zoster ophthalmicus ? iritis, iridocyclitis ? chorioretinitis ? diffuse posterior uveitis and choroiditis ? optic neuritis ? sympathetic ophthalmia ? anterior segment inflammation ? allergic conjunctivitis ? allergic corneal marginal ulcers ? keratitis.,7. gastrointestinal diseases to tide the patient over a critical period of the disease in: ? ulcerative colitis (systemic therapy) ? regional enteritis (systemic therapy).,8. respiratory diseases ? symptomatic sarcoidosis ? loeffler's syndrome not manageable by other means ? berylliosis ? fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy ? aspiration pneumonitis.,9. haematological disorders ? acquired (autoimmune) haemolytic anaemia ? erythroblastopenia (rbc anaemia) ? idiopathic thrombocytopenic purpura in adults (iv only; im administration is contraindicated) ? secondary thrombocytopenia in adults ? congenital (erythroid) hypoplastic anaemia.,10. neoplastic diseases for palliative management of: ? leukaemias and lymphomas in adults ? acute leukaemia in childhood.,11. oedematous states ? to induce diuresis or remission of proteinuria in the nephrotic syndrome, without uraemia, of the idiopathic type or that due to lupus erythematosus.,12. miscellaneous ? tuberculous meningitis with subarachnoid block or impending block when used concurrently with appropriate antituberculous chemotherapy ? trichinosis with neurological or myocardial involvement.

Urostemol Prosta capsules Regno Unito - inglese - myHealthbox

urostemol prosta capsules

omega pharma ltd - pumpkin seed soft extract - capsule, hard. - 500 mg - a traditional herbal medicinal product used for the relief of lower urinary tract symptoms in men related to an overactive bladder, such as urgency to urinate and frequent urination, or who have a confirmed diagnosis of benign prostatic hyperplasia (bph), based on traditional use only.

Urostemol Men capsules Regno Unito - inglese - myHealthbox

urostemol men capsules

omega pharma ltd - pumpkin seed, crushed , pumpkin seed oil, extract from saw palmetto fruit - capsule, hard. - 400 mg, 340 mg, 75 mg - a traditional herbal medicinal product used for the relief of lower urinary tract symptoms in men related to an overactive bladder or bladder weakness, such as urgency to urinate, urinary incontinence, frequent urination day and night based on traditional use only.

Urostemol femina capsules Regno Unito - inglese - myHealthbox

urostemol femina capsules

omega pharma ltd - pumpkin seed oil, dry extract of fragrant sumach bark, dry extract of hop strobile - capsule, hard. - 227.3 mg, 56 mg, 18 mg - a traditional herbal medicinal product used for the relief of lower urinary tract symptoms in women related to an overactive bladder or bladder weakness, such as urgency to urinate, urinary incontinence, frequent urination based on traditional use only.

Urostemol capsules Regno Unito - inglese - myHealthbox

urostemol capsules

omega pharma ltd - pumpkin seed, crushed, pumpkin seed oil - capsule, hard. - 400 mg, 340 mg - a traditional herbal medicinal product used for the relief of lower urinary tract symptoms related to an overactive bladder or bladder weakness, such as urgency to urinate, urinary incontinence, frequent urination, based on traditional use only.

SODIUM ACETATE INJECTION USP SOLUTION Canada - inglese - Health Canada

sodium acetate injection usp solution

omega laboratories limited - sodium acetate - solution - 328mg - sodium acetate 328mg - replacement preparations