GOUTIFADE 80MG 20TAB

each goutifade 80 mg film coated tablet contains 80 mg of febuxostat .

48.00 EGP

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GOUTIFADE 80MG 20TAB ; febuxostat, antigout agents

GOUTIFADE 80MG 20TAB

ACTIVE-INGREDIENT OF GOUTIFADE 80MG 20TAB

each goutifade 80 mg film coated tablet contains 80 mg of febuxostat .

INDICATION

goutifade is a xanthine oxidase (XO) inhibitor indicated for the chronic management of hyperuricemia in patients with gout .

Goutifade is not recommended for the treatment of asymptomatic hyperuricemia

DOSAGE

Follow all directions given to you by your pharmacist or doctor carefully . They may differ from the information contained in this leaflet

Ask your pharmacist or doctor for help if you do not understand the instructions on the box .

The recommended dose is : –

recommended dose : for the treatment of hyperuricemia in patients with gout , goutifade , febuxostat is recommendedat 40 mg or 80 mg once daily .

The recommended starting dose of goutifade , febuxostat is 40 mg once daily . F

or patients who do not achieve a serum uric acid (sUA) less than 6 mg /dl after two weeks with 40 mg , goutifade 80 mg , febuxostat is recommended . goutifade , febuxostat can be taken without regard to food or antacid use . special populations : no dose adjustment is necessary when administering goutifade , febuxostat in patients with mild to moderate renal impairment . the recommended starting dose of goutifade , febuxostat is 40 mg once daily .

for patients who do not achieve a sUA less than 6 mg/dl after two weeks with 40 mg , goutifade 80 mg , febuxostat is recommended . no dose adjustment is necessary in patients with mild to moderate hepatic impairment . uric acid level: testing for the target serum uric acid level of less than 6 mg/dl may be performed as early as two weeks after initiating goutifade therapy .

gout flares : gout flares may occur after initiation of goutifade due to changing serum acid levels resulting in mobilization of urate from tissue deposits .

if a gout flare occurs during goutifade treatment , goutifade need not be discontinued .

OVER-DOSAGE

Before starting to use the medicine, that is, any medicine, or the pharmacist
Cancer in medicine before using this medicine

CONTRA-INDICATION

hypersensitiviity to the active substance or to any of the excipients .
Febuxostat is contraindicated in patients receiving azathioprine

STORAGE OF 

Store at temperature not exceeding 30°C, in dry place.
PACK
carton box containing 2 or 3 (white opaque aclar/pvc/al) strips of 10 film coated tablets & an inner leaflet .
MANUFACTURED
GLOBAL NAPI PHARMACEUTICALS

https://www.webmd.com/drugs/2/drug-151868/febuxostat-oral/details

https://www.gardeniapharmacy.com/category/medicine-2/

 

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