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

ABDOMINAL PAIN UPPER ( 6 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
FALL ( 3 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
TREMOR ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
ILEUS ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
ABASIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEATH ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
CRYING ( 1 FDA reports)
COUGH ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
RALES ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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