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

MYOCARDIAL INFARCTION ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
ENCEPHALOPATHY ( 5 FDA reports)
ARTHRALGIA ( 4 FDA reports)
DEPRESSED MOOD ( 4 FDA reports)
AGGRESSION ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
METABOLIC SYNDROME ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
ABASIA ( 2 FDA reports)
AGITATION ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
FALL ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
RASH ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ANGER ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORNEAL LESION ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FRONTAL LOBE EPILEPSY ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SURGERY ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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