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

GASTROINTESTINAL DISORDER ( 20 FDA reports)
MULTI-ORGAN DISORDER ( 20 FDA reports)
IRRITABLE BOWEL SYNDROME ( 20 FDA reports)
INTESTINAL HAEMORRHAGE ( 20 FDA reports)
PROCTITIS ULCERATIVE ( 20 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 20 FDA reports)
COLITIS ( 20 FDA reports)
COLITIS ULCERATIVE ( 20 FDA reports)
HEADACHE ( 20 FDA reports)
PROCTOCOLITIS ( 20 FDA reports)
NERVOUSNESS ( 20 FDA reports)
RECTAL HAEMORRHAGE ( 20 FDA reports)
EPISTAXIS ( 20 FDA reports)
HAEMORRHOIDS ( 10 FDA reports)
IRON DEFICIENCY ANAEMIA ( 7 FDA reports)
AGITATION ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
ARTHRALGIA ( 5 FDA reports)
VIRAL INFECTION ( 5 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
FAECAL INCONTINENCE ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
TONSILLAR HYPERTROPHY ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
HAEMATOCRIT INCREASED ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
INJURY ( 2 FDA reports)
POLYTRAUMATISM ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
NAUSEA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
LACERATION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
VOMITING ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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