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PHARMACEUTICAL PRODUCT COMPLAINT ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
CARDIAC MYXOMA ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
PAIN ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BONE SARCOMA ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST WALL OPERATION ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIABETIC BULLOSIS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PSEUDOMYXOMA PERITONEI ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RECALL PHENOMENON ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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