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

ABNORMAL BEHAVIOUR ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 3 FDA reports)
TACHYARRHYTHMIA ( 3 FDA reports)
PALLOR ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
INCOHERENT ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
PURPURA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
COUGH ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
RASH ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)

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