Remicade New Zealand - English - Medsafe (Medicines Safety Authority)

remicade

janssen-cilag (new zealand) ltd - infliximab 100mg;   - powder for injection - 100 mg - active: infliximab 100mg   excipient: dibasic sodium phosphate dihydrate monobasic sodium phosphate monohydrate polysorbate 80 sucrose - rheumatoid arthritis remicade is a ?disease-controlling anti-rheumatic therapy" (dcart) indicated for: · the reduction of signs and symptoms · prevention of structural joint damage (erosions and joint space narrowing) · improvement in physical function in patients with active disease. remicade should be given in combination with methotrexate.

Ribomustin 100mg 100 mg Jordan - English - JFDA (Jordan Food & Drug Administration - المؤسسة العامة للغذاء والدواء)

ribomustin 100mg 100 mg

مستودع أدوية ابن رشد - ibn rushd drug store - bendamustine hydrochloride 100 mg - 100 mg

VECAMYL- mecamylamine hydrochloride tablet United States - English - NLM (National Library of Medicine)

vecamyl- mecamylamine hydrochloride tablet

vyera pharmaceuticals, llc - mecamylamine hydrochloride (unii: 4956djr58o) (mecamylamine - unii:6ee945d3ok) - mecamylamine hydrochloride 2.5 mg - for the management of moderately severe to severe essential hypertension and in uncomplicated cases of malignant hypertension. mecamylamine hcl should not be used in mild, moderate, labile hypertension and may prove unsuitable in uncooperative patients. it is contraindicated in coronary insufficiency or recent myocardial infarction. mecamylamine hcl should be given with great discretion, if at all, when renal insufficiency is manifested by a rising or elevated bun. the drug is contraindicated in uremia. patients receiving antibiotics and sulfonamides should generally not be treated with ganglion blockers. other contraindications are glaucoma, organic pyloric stenosis or hypersensitivity to the product.

DIANEAL PD-2 WITH DEXTROSE- sodium chloride, sodium lactate, calcium chloride, magnesium chloride and dextrose injection, soluti United States - English - NLM (National Library of Medicine)

dianeal pd-2 with dextrose- sodium chloride, sodium lactate, calcium chloride, magnesium chloride and dextrose injection, soluti

baxter healthcare corporation - dextrose monohydrate (unii: lx22yl083g) (anhydrous dextrose - unii:5sl0g7r0ok), sodium chloride (unii: 451w47iq8x) (sodium cation - unii:lyr4m0nh37, chloride ion - unii:q32zn48698), sodium lactate (unii: tu7hw0w0qt) (sodium cation - unii:lyr4m0nh37, lactic acid - unii:33x04xa5at), calcium chloride (unii: m4i0d6vv5m) (calcium cation - unii:2m83c4r6zb, chloride ion - unii:q32zn48698), magnesium chloride (unii: 02f3473h9o) (magnesium cation - unii:t6v3lhy838, chloride ion - unii:q32zn48698) - dextrose monohydrate 1.5 g in 100 ml - dianeal peritoneal dialysis solutions are indicated for patients in acute or chronic renal failure. dianeal peritoneal dialysis solutions are contraindicated in patients with severe lactic acidosis. dianeal peritoneal dialysis solution is a pharmacologically inactive solution. while there are no adequate and well controlled studies in pregnant women, appropriate administration of dianeal solutions, with appropriate monitoring of hematology, electrolytes, blood chemistry and fluid status is not expected to cause fetal harm. animal reproduction studies have not been conducted with dianeal solutions. the estimated background risk of major birth defects and miscarriage for the indicated population is unknown. in the u.s. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2-4% and 15-20%, respectively. the components of dianeal solutions are excreted in human milk. safety and effectiveness have been established based on published clinic

CHILDRENS IBUPROFEN- ibuprofen suspension United States - English - NLM (National Library of Medicine)

childrens ibuprofen- ibuprofen suspension

valu merchandisers company - ibuprofen (unii: wk2xyi10qm) (ibuprofen - unii:wk2xyi10qm) - ibuprofen 100 mg in 5 ml - pain reliever/fever reducer temporarily: - relieves minor aches and pains due to the common cold, flu, sore throat, headache and toothache - reduces fever - if the child has ever had an allergic reaction to any other pain reliever/fever reducer - right before or after heart surgery - stomach bleeding warning applies to your child - child has a history of stomach problems, such as heartburn - child has problems or serious side effects from taking pain relievers or fever reducers - child has not been drinking fluids - child has lost a lot of fluid due to vomiting or diarrhea - child has high blood pressure, heart disease, liver cirrhosis, or kidney disease - child has asthma - child is taking a diuretic - under a doctor’s care for any serious condition - taking any other drug - child experiences any of the following signs of stomach bleeding feels faint vomits blood has bloody or black stools has stomach pain that does not get better - feels faint - vomits blood - has bloody or

Setrona New Zealand - English - Medsafe (Medicines Safety Authority)

setrona

douglas pharmaceuticals limited - sertraline hydrochloride 111.92mg equivalent to sertraline 100 mg;  ;   - film coated tablet - 100 mg - active: sertraline hydrochloride 111.92mg equivalent to sertraline 100 mg     excipient: calcium hydrogen phosphate dihydrate hyprolose magnesium stearate microcrystalline cellulose opadry white oy-s-58910 sodium starch glycolate - setrona is indicated for the treatment of paediatric patients (6- 17 years of age) with ocd. setrona is indicated for the treatment of obsessive-compulsive disorder (ocd).

Zoloft New Zealand - English - Medsafe (Medicines Safety Authority)

zoloft

viatris limited - sertraline hydrochloride 111.9mg equivalent to 100 mg sertraline;  ;   - film coated tablet - 100 mg - active: sertraline hydrochloride 111.9mg equivalent to 100 mg sertraline     excipient: calcium hydrogen phosphate hyprolose magnesium stearate microcrystalline cellulose opadry clear ys-1-7006 opadry white ys-1r-7003 purified water   sodium starch glycolate

ANIMAL PATHOGENS NOSODE COMBINATION 9419- animal pathogens nosode combination liquid United States - English - NLM (National Library of Medicine)

animal pathogens nosode combination 9419- animal pathogens nosode combination liquid

professional complementary health formulas - baptisia tinctoria 3x gelsemium sempervirens 3x ignatia amara 6x phosphorus 6x pasteurellose 12x tularemia 12x - for the temporary relief of occasional headache, minor muscle or joint pain, fatigue, or skin irritations.* *claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

PROTEUS NOSODE COMBINATION 9415- proteus nosode combination liquid United States - English - NLM (National Library of Medicine)

proteus nosode combination 9415- proteus nosode combination liquid

professional complementary health formulas - gelsemium sempervirens 3x colchicum autumnale 4x colocynthis 6x nux vomica 6x bacillus proteus 12x mercurius corrosivus 12x - for the temporary relief of urinary discomfort, difficulty or increased frequency, minor back pain, fatigue, nausea, vomiting, or diarrhea.* *claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

URINARY NOSODE COMBINATION 9410- urinary nosode combination liquid United States - English - NLM (National Library of Medicine)

urinary nosode combination 9410- urinary nosode combination liquid

professional complementary health formulas - terebinthina 4x ononis spinosa 6x cantharis 8x berberis vulgaris 10x bacillus morgan 12x leptospirosis 12x - for the temporary relief of urinary discomfort or difficulty, minor abdominal or back pain, occasional headache, fatigue, nausea, vomiting, or diarrhea.* *claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.