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

INSOMNIA ( 3 FDA reports)
VOMITING ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
MENISCUS LESION ( 2 FDA reports)
FALL ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
ATROPHY ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
ANTICONVULSANT TOXICITY ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
ANGER ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
PYELECTASIA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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