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

PNEUMONIA ( 7 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
AGITATION ( 5 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
FALL ( 4 FDA reports)
SYNCOPE ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
ABASIA ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
PLICATED TONGUE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
CRYING ( 2 FDA reports)
DEATH ( 2 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
SENILE DEMENTIA ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
TESTICULAR RETRACTION ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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