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

DIZZINESS ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OESOPHAGEAL DISORDER ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TREMOR ( 2 FDA reports)
AGITATION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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