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

FALL ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
SYNCOPE ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
PATELLA FRACTURE ( 2 FDA reports)
GRUNTING ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DELIRIUM ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
STRESS ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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