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

RENAL FAILURE ACUTE ( 6 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
VOMITING ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
NARCOTIC INTOXICATION ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
MALAISE ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
MONONEUROPATHY ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
ORTHOSIS USER ( 1 FDA reports)
PHYSIOTHERAPY ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)

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