KUWAIT DRUGS

 

SEARCH

 

SUGGESTIONS

 

ADD PRODUCTS

 

HOME

0-9    A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

 

 

PREVIOUS

  

NEXT

 
 

RELIFEX 500 MG TABLETS

 

 
 

 

GENERIC NAMES

MANUFACTURERS 

MEDICAL GROUP

MEDICAL ARTICLES

 

DRUGS IN :

 

 

FDA DRUGS

UNITED STATES

CANADA

UNITED KINGDOM

AUSTRALIA

GERMANY

FRANCE

MIDDLE EAST

KUWAIT

LEBANON

EGYPT

SYRIA

BAHRAIN

IRAN

JORDAN

SAUDI ARABIA

UNITED ARAB EMIRATES

 

 

 
 

SIZE:

500 MG

 

GENERIC NAME:

NABUMETONE

 

MANUFACTURER:

SMITH KLINE BEECHAM

 

UNIT:

 

ADMINISTRATION ROUTE:

 

FDA PREGNANCY GROUP:

C

 

INDICATIONS:

Arthritis, osteoarthritis

Arthritis, rheumatoid

 

SIDE EFFECTS:

abdominal pain

agitation

anaphylactic shock

anaphylactoid reactions

anemia

angina

angioedema

anorexia

anxiety

aseptic meningitis

asthenia

azotemia

blurred vision

bullous rash

confusion

constipation

depression

diaphoresis

diarrhea

dizziness

dyspepsia

dysphagia

edema

elevated hepatic enzymes

eosinophilia

eructation

erythema multiforme

esophageal stricture

esophageal ulceration

esophagitis

fatigue

flatulence

gastritis

GI bleeding

GI perforation

headache

heart failure

hematuria

hepatic failure

hepatitis

hyperkalemia

hypertension

hyperuricemia

insomnia

interstitial nephritis

jaundice

leukopenia

malaise

melena

myocardial infarction

nausea/vomiting

nephrotic syndrome

odynophagia

palpitations

pancreatitis

paresthesias

peptic ulcer

photosensitivity

platelet dysfunction

pneumonitis

proteinuria

pruritus

pseudoporphyria

pyrosis (heartburn)

rash (unspecified)

renal failure (unspecified)

renal papillary necrosis

Stevens-Johnson syndrome

syncope

thrombocytopenia

tinnitus

toxic epidermal necrolysis

tremor

urticaria

vasculitis

vertigo

visual impairment

xerostomia

 

ABSOLUTE CONTRAINDICATIONS :

 

RELATIVE CONTRAINDICATIONS :

acute bronchospasm

alcoholism

anemia

anticoagulant therapy

asthma

bone marrow suppression

breast-feeding

cardiac disease

cerebrovascular disease

chemotherapy

coagulopathy

corticosteroid therapy

dehydration

dental disease

dental work

diabetes mellitus

edema

elderly

GI bleeding

GI disease

heart failure

hematological disease

hemophilia

hepatic disease

hypertension

hypovolemia

immunosuppression

intramuscular injections

jaundice

labor

myocardial infarction

nasal polyps

neutropenia

peptic ulcer disease

peripheral edema

peripheral vascular disease

pregnancy

renal disease

renal failure

renal impairment

rheumatoid arthritis

stroke

surgery

systemic lupus erythematosus (SLE)

thrombocytopenia

tobacco smoking

ulcerative colitis

 

ADULT DOSE:

Antirheumatic (nonsteroidal anti-inflammatory) -Oral, initially 1000 mg a day, as a single dose (usually at night) or in two divided doses (in the morning and evening). Dosage may be increased, if necessary, to 1500 mg or 2000 mg a day in two divided doses. After a satisfactory response has been obtained, dosage should be individualized according to patient tolerance and response. The lowest dose that provides continuing control of symptoms should be used for maintenance.

 

MAXIMUM ADULT DOSE:

Doses larger than 2000 mg a day have not been studied and are not recommended.

 

PEDIATRIC DOSE:

Safety and efficacy have not been established .  

 

MAXIMUM PEDIATRIC DOSE:

 

ELDERLY DOSE:

Antirheumatic (nonsteroidal anti-inflammatory) -Oral, initially 1000 mg a day, as a single dose (usually at night) or in two divided doses (in the morning and evening). Dosage may be increased, if necessary, to 1500 mg or 2000 mg a day in two divided doses. After a satisfactory response has been obtained, dosage should be individualized according to patient tolerance and response. The lowest dose that provides continuing control of symptoms should be used for maintenance.

 

 

PREVIOUS

  

NEXT