Invanz Uusi-Seelanti - englanti - Medsafe (Medicines Safety Authority)

invanz

merck sharp & dohme (new zealand) limited - ertapenem sodium 209.2 mg/ml equivalent to 200 mg/ml ertapenem free acid - powder for injection - 200 mg/ml - active: ertapenem sodium 209.2 mg/ml equivalent to 200 mg/ml ertapenem free acid excipient: sodium bicarbonate sodium hydroxide water for injection - treatment invanz is indicated for the treatment of patients with moderate to severe infections caused by susceptible strains of micro-organisms, as well as initial empiric therapy prior to the identification of causative organisms in the infections listed below: · complicated intra-abdominal infections · complicated skin and skin structure infections including diabetic lower extremity and diabetic foot infections · community acquired pneumonia · complicated urinary tract infections including pyelonephritis · acute pelvic infections including postpartum endomyometritis, septic abortion and post-surgical gynaecologic infections · bacterial septicaemia prevention invanz is indicated in adults for the prophylaxis of surgical site infection following elective colorectal surgery.

OncoTICE Uusi-Seelanti - englanti - Medsafe (Medicines Safety Authority)

oncotice

merck sharp & dohme (new zealand) limited - bacillus calmette-guerin 500 mcfu (range: 2-8x10e8 cfu) - powder for injection - 500 mcfu - active: bacillus calmette-guerin 500 mcfu (range: 2-8x10e8 cfu) excipient: ammonia solution asparagine citric acid monohydrate dibasic potassium phosphate ferric ammonium citrate glycerol zinc formate lactose magnesium sulfate - oncotice is used as a treatment of flat urothelial cell carcinoma in situ (cis) of the bladder, and as an adjuvant therapy after transurethral resection (tur) of a primary or relapsing superficial papillary urothelial cell carcinoma of the bladder stage ta (grade 2 or 3) or t1 (grade 1, 2 or 3). oncotice is only recommended for stage ta grade 1 papillary tumours when there is judged to be a high risk of tumour recurrence.

Pneumovax 23 vaccine Uusi-Seelanti - englanti - Medsafe (Medicines Safety Authority)

pneumovax 23 vaccine

merck sharp & dohme (new zealand) limited - pneumococcal polysaccharide vaccine 50 µg/ml (25mcg/dose of each of 23 named pneumococcal polysaccharides) - solution for injection - active: pneumococcal polysaccharide vaccine 50 µg/ml (25mcg/dose of each of 23 named pneumococcal polysaccharides) excipient: phenol sodium chloride water for injection - pneumovax 23 is indicated for vaccination against pneumococcal disease caused by those pneumococcal types included in the vaccine.

Stocrin Uusi-Seelanti - englanti - Medsafe (Medicines Safety Authority)

stocrin

merck sharp & dohme (new zealand) limited - efavirenz 200mg - film coated tablet - 200 mg - active: efavirenz 200mg excipient: carnauba wax croscarmellose sodium hypromellose lactose monohydrate magnesium stearate microcrystalline cellulose opadry yellow 03b12896 sodium laurilsulfate - stocrin is indicated in antiviral combination treatment of hiv-1 infected adults, adolescents and children.

Stocrin Uusi-Seelanti - englanti - Medsafe (Medicines Safety Authority)

stocrin

merck sharp & dohme (new zealand) limited - efavirenz 300mg;  ;   - film coated tablet - 300 mg - active: efavirenz 300mg     excipient: carnauba wax croscarmellose sodium hyprolose lactose monohydrate magnesium stearate microcrystalline cellulose opadry clear ys-1-19025-a opadry white ys-1-18177-a purified water   sodium laurilsulfate

Stocrin Uusi-Seelanti - englanti - Medsafe (Medicines Safety Authority)

stocrin

merck sharp & dohme (new zealand) limited - efavirenz 50mg - film coated tablet - 50 mg - active: efavirenz 50mg excipient: carnauba wax croscarmellose sodium hypromellose lactose monohydrate magnesium stearate microcrystalline cellulose opadry yellow 03b12896 sodium laurilsulfate

Stocrin Uusi-Seelanti - englanti - Medsafe (Medicines Safety Authority)

stocrin

merck sharp & dohme (new zealand) limited - efavirenz 600mg - film coated tablet - 600 mg - active: efavirenz 600mg excipient: carnauba wax croscarmellose sodium hyprolose lactose monohydrate magnesium stearate microcrystalline cellulose opadry yellow 03b12896 purified water   sodium laurilsulfate - stocrin is indicated in antiviral combination treatment of hiv-1 infected adults, adolescents and children

Stromectol Uusi-Seelanti - englanti - Medsafe (Medicines Safety Authority)

stromectol

merck sharp & dohme (new zealand) limited - ivermectin 3mg - tablet - 3 mg - active: ivermectin 3mg excipient: butylated hydroxyanisole citric acid magnesium stearate microcrystalline cellulose starch - · treatment of intestinal strongyloidiasis (anguillulosis). · treatment of proven suspected microfilaraemia in patients with lymphatic filariasis caused by wuchereria bancrofti. · treatment of human sarcoptic scabies after prior treatment has failed. treatment is justified when the diagnosis of scabies has been established clinically and/or by parasitological examination. without formal diagnosis, treatment is not justified in case of pruritus.

JANUMET™ Tablet 50mg1000mg Singapore - englanti - HSA (Health Sciences Authority)

janumet™ tablet 50mg1000mg

msd pharma (singapore) pte. ltd. - metformin hydrochloride; sitagliptin phosphate monohydrate 64.25mg eqv sitagliptin - tablet, film coated - 1000.0 mg - metformin hydrochloride 1000.0 mg; sitagliptin phosphate monohydrate 64.25mg eqv sitagliptin 50 mg