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

DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
PARAESTHESIA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
BLISTER ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
ULCER ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
FOETAL DISORDER ( 2 FDA reports)
FALL ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
ABORTION SPONTANEOUS COMPLETE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
CHOREA ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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