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

COMPLETED SUICIDE ( 9 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
POISONING ( 5 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
DYSTONIA ( 4 FDA reports)
AKINESIA ( 3 FDA reports)
APHASIA ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
OCULOGYRIC CRISIS ( 3 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CRYING ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HIRSUTISM ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYCYSTIC OVARIES ( 2 FDA reports)
STRESS URINARY INCONTINENCE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COMA ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RECTAL PERFORATION ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DYSKINESIA ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SURGERY ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THEFT ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TIC ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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