Please choose an event type to view the corresponding MedsFacts report:

ANAEMIA ( 5 FDA reports)
MELAENA ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
VOMITING ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
CUSHINGOID ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FALL ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
GASTRODUODENITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INJURY ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
COMA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OSTEOCHONDROMA ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
RASH ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SOPOR ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)

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