Ireland - English - HPRA (Health Products Regulatory Authority)

ethypharm - hydromorphone hydrochloride - solution for injection/infusion - 50 milligram(s)/millilitre - natural opium alkaloids; hydromorphone

United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

martindale pharmaceuticals ltd - morphine sulfate - solution for infusion - 2mg/1ml

United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

martindale pharmaceuticals ltd - morphine sulfate - solution for infusion - 1mg/1ml

Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

rwr veterinary products pty ltd - glucose; calcium carbonate; methandriol dipropionate; vitamin b3 = nicotinamide; vitamin b5 calcium salt = calcium pantothenate; vitamin b2 = riboflavin; vitamin b1 hydrochloride = thiamine hydrochloride; vitamin b6 hydrochloride = pyridoxine hydrochloride; vitamin e-d = alpha tocopherol-d; yeast dried - oral powder, pre-mix - glucose carbohydrate active 384.8 g/kg; calcium carbonate mineral-calcium-salt active 280.0 g/kg; methandriol dipropionate steroid-anabolic active 1.2 g/kg; vitamin b3 = nicotinamide vitamin-b3 active 1.5 g/kg; vitamin b5 calcium salt = calcium pantothenate vitamin-b5 active 5.0 g/kg; vitamin b2 = riboflavin vitamin-b2 active 2.5 g/kg; vitamin b1 hydrochloride = thiamine hydrochloride vitamin-b1 active 5.0 g/kg; vitamin b6 hydrochloride = pyridoxine hydrochloride vitamin-b6 active 5.0 g/kg; vitamin e-d = alpha tocopherol-d vitamin-e active 17.5 g/kg; yeast dried biological-organism-fungus active 280.0 g/kg - endocrine system - dog | horse | horse - adult | horse - yearling | horse weanling | bitch | castrate | colt | donkey | endurance horse | filly | f - calcium supplement | vitamin deficiency | prevention & treatment of anae | treatment of basal metabolic d | treatment of debility & anorex

Canada - English - Health Canada

emd serono, a division of emd inc., canada - somatropin; sodium chloride - powder for solution - 3.3mg; 5ml - somatropin 3.3mg; sodium chloride 5ml - pituitary

Canada - English - Health Canada

emd serono, a division of emd inc., canada - somatropin - powder for solution - 5mg - somatropin 5mg - pituitary

Canada - English - Health Canada

emd serono, a division of emd inc., canada - somatropin - powder for solution - 8.8mg - somatropin 8.8mg - pituitary

Australia - English - Department of Health (Therapeutic Goods Administration)

hospira australia pty ltd - sodium nitroprusside -

Israel - English - Ministry of Health

roche pharmaceuticals (israel) ltd - atezolizumab - concentrate for solution for infusion - atezolizumab 60 mg/ml - urothelial carcinoma• tecentriq (atezolizumab) is indicated for the treatment of patients with locally advanced or metastatic urothelial carcinoma who are not eligible for cisplatin-containing chemotherapy and whose tumours have a pd-l1 expression ≥ 5%.• tecentriq is indicated for the treatment of patients with locally advanced or metastatic urothelial carcinoma who have disease progression during or following any platinum-containing chemotherapy, or within 12 months of neoadjuvant or adjuvant chemotherapy.- non-small cell lung cancer •tecentriq, as a single agent, is indicated for the first-line treatment of adult patients with metastatic non-small cell lung cancer (nsclc) whose tumors have high pd-l1 expression (pd-l1 stained ≥ 50% of tumor cells [tc ≥ 50%] or pd-l1 stained tumor-infiltrating immune cells [ic] covering ≥ 10% of the tumor area [ic ≥ 10%]), as determined by an approved test, with no egfr or alk genomic tumor aberrations.•tecentriq, in combination with paclitaxel protein-bound and carboplatin, is indicated for the first-line treatment of adult patients with metastatic non-squamous nsclc with no egfr or alk genomic tumor aberrations.• tecentriq, in combination with bevacizumab, paclitaxel, and carboplatin, is indicated for the first-line treatment of adult patients with metastatic non-squamous non-small cell lung cancer (nsclc). in patients with egfr mutant or alk-positive nsclc, tecentriq, in combination with bevacizumab, paclitaxel, and carboplatin, is indicated only after failure of appropriate targeted therapies.• tecentriq is indicated for the treatment of patients with metastatic nsclc who are naïve to anti-pd-l1 or anti-pd-1 therapies and have disease progression during or following platinum-containing chemotherapy. patients with egfr or alk genomic tumor aberrations should have disease progression on approved therapy for nsclc harboring these aberrations prior to receiving tecentriq.• tecentriq as monotherapy, is indicated as adjuvant treatment following complete resection and no progression after platinum-based adjuvant chemotherapy for adult patients with stage ii to iiia nsclc whose tumors have pd-l1 expression on ≥ 50% of tumor cells (tcs).- locally advanced or metastatic triple-negative breast cancer tecentriq, in combination with nab-paclitaxel, is indicated for the treatment of patients with unresectable locally advanced or metastatic triple-negative breast cancer (tnbc) whose tumors have pd-l1 expression ≥1% and who have not received prior chemotherapy for metastatic disease.- small cell lung cancertecentriq, in combination with carboplatin and etoposide, is indicated for the first-line treatment of adult patients with extensive-stage small cell lung cancer (es-sclc)."- hepatocellular carcinomatecentriq, in combination with bevacizumab, is indicated for the treatment of patients with unresectable or metastatic hepatocellular carcinoma (hcc) who have not received prior systemic therapy.- melanomatecentriq, in combination with cobimetinib and vemurafenib, is indicated for the treatment of patients with braf v600 mutation-positive unresectable or metastatic melanoma.- alveolar soft part sarcoma tecentriq, as a single agent, is indicated for the treatment of adult and pediatric patients 2 years of age and older with unresectable or metastatic alveolar soft part sarcoma (asps).