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

NEUTROPENIA ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
INSOMNIA ( 3 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
THYROID CANCER ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
RASH ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
COMA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EXHIBITIONISM ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
CARCINOID SYNDROME ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)

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