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

ALOPECIA ( 6 FDA reports)
ULCER HAEMORRHAGE ( 6 FDA reports)
HYPOTRICHOSIS ( 6 FDA reports)
HEADACHE ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
BRONCHITIS ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
EAR INFECTION ( 4 FDA reports)
TINNITUS ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 3 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
URETHRAL SPASM ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
PAIN ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HOUSE DUST ALLERGY ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
MASTOIDITIS ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
DRUG USE FOR UNKNOWN INDICATION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VOMITING ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)

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