Granisetron 2mg tablets Suurbritannia - inglise - MHRA (Medicines & Healthcare Products Regulatory Agency)

granisetron 2mg tablets

apc pharmaceuticals & chemicals (europe) ltd - granisetron hydrochloride - oral tablet - 2mg

Granisetron 2mg tablets Suurbritannia - inglise - MHRA (Medicines & Healthcare Products Regulatory Agency)

granisetron 2mg tablets

alliance healthcare (distribution) ltd - granisetron hydrochloride - oral tablet - 2mg

Granisetron 2mg tablets Suurbritannia - inglise - MHRA (Medicines & Healthcare Products Regulatory Agency)

granisetron 2mg tablets

sigma pharmaceuticals plc - granisetron hydrochloride - oral tablet - 2mg

Granisetron 2mg tablets Suurbritannia - inglise - MHRA (Medicines & Healthcare Products Regulatory Agency)

granisetron 2mg tablets

cubic pharmaceuticals ltd - granisetron hydrochloride - oral tablet - 2mg

Granisetron 2mg tablets Suurbritannia - inglise - MHRA (Medicines & Healthcare Products Regulatory Agency)

granisetron 2mg tablets

colorama pharmaceuticals ltd - granisetron hydrochloride - oral tablet - 2mg

Granisetron 1mg tablets Suurbritannia - inglise - MHRA (Medicines & Healthcare Products Regulatory Agency)

granisetron 1mg tablets

apc pharmaceuticals & chemicals (europe) ltd - granisetron hydrochloride - oral tablet - 1mg

GRANISETRON HYDROCHLORIDE tablet, film coated Ameerika Ühendriigid - inglise - NLM (National Library of Medicine)

granisetron hydrochloride tablet, film coated

orchidpharma inc - granisetron hydrochloride (unii: 318f6l70j8) (granisetron - unii:wzg3j2mcol) - granisetron 1 mg - granisetron hydrochloride tablets are indicated for the prevention of: - nausea and vomiting associated with initial and repeat courses of emetogenic cancer therapy, including high-dose cisplatin. - nausea and vomiting associated with radiation, including total body irradiation and fractionated abdominal radiation. granisetron hydrochloride is contraindicated in patients with known hypersensitivity to the drug or any of its components.