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

SEPSIS ( 12 FDA reports)
HYPOTENSION ( 11 FDA reports)
PURULENT DISCHARGE ( 11 FDA reports)
COAGULOPATHY ( 10 FDA reports)
INFECTION ( 10 FDA reports)
THROMBOCYTOPENIA ( 10 FDA reports)
ABSCESS NECK ( 9 FDA reports)
ADDISON'S DISEASE ( 9 FDA reports)
ADRENAL INSUFFICIENCY ( 9 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 9 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 9 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 9 FDA reports)
ATELECTASIS ( 9 FDA reports)
ATRIAL FIBRILLATION ( 9 FDA reports)
BIOPSY BONE ABNORMAL ( 9 FDA reports)
BONE DISORDER ( 9 FDA reports)
CANDIDIASIS ( 9 FDA reports)
CARDIAC ARREST ( 9 FDA reports)
CARDIAC DISORDER ( 9 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 9 FDA reports)
CARDIOMEGALY ( 9 FDA reports)
CARDIOVASCULAR DISORDER ( 9 FDA reports)
CATARACT ( 9 FDA reports)
CATHETERISATION CARDIAC ( 9 FDA reports)
CELLULITIS ( 9 FDA reports)
CONTUSION ( 9 FDA reports)
CORONARY ARTERY DISEASE ( 9 FDA reports)
DEAFNESS ( 9 FDA reports)
DECREASED APPETITE ( 9 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 9 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 9 FDA reports)
DILATATION VENTRICULAR ( 9 FDA reports)
DIPLOPIA ( 9 FDA reports)
DYSGEUSIA ( 9 FDA reports)
DYSPHAGIA ( 9 FDA reports)
EDENTULOUS ( 9 FDA reports)
EJECTION FRACTION DECREASED ( 9 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 9 FDA reports)
EXTREMITY NECROSIS ( 9 FDA reports)
FACIAL PAIN ( 9 FDA reports)
FANCONI SYNDROME ( 9 FDA reports)
GAIT DISTURBANCE ( 9 FDA reports)
HEPATIC ENZYME ABNORMAL ( 9 FDA reports)
HIP FRACTURE ( 9 FDA reports)
HYPERKALAEMIA ( 9 FDA reports)
HYPERPARATHYROIDISM ( 9 FDA reports)
HYPOKALAEMIA ( 9 FDA reports)
IMPAIRED HEALING ( 9 FDA reports)
INFLAMMATION ( 9 FDA reports)
JAW FRACTURE ( 9 FDA reports)
JOINT CREPITATION ( 9 FDA reports)
JOINT DISLOCATION ( 9 FDA reports)
KLEBSIELLA INFECTION ( 9 FDA reports)
KYPHOSCOLIOSIS ( 9 FDA reports)
LYMPHADENOPATHY ( 9 FDA reports)
MALNUTRITION ( 9 FDA reports)
MASTICATION DISORDER ( 9 FDA reports)
MITRAL VALVE INCOMPETENCE ( 9 FDA reports)
MYELOMA RECURRENCE ( 9 FDA reports)
MYOCLONUS ( 9 FDA reports)
NEUROPATHY PERIPHERAL ( 9 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 9 FDA reports)
ORAL CAVITY FISTULA ( 9 FDA reports)
ORTHOSTATIC HYPOTENSION ( 9 FDA reports)
OSTEOLYSIS ( 9 FDA reports)
OSTEOMYELITIS ( 9 FDA reports)
OSTEONECROSIS OF JAW ( 9 FDA reports)
OSTEOPENIA ( 9 FDA reports)
OSTEOSCLEROSIS ( 9 FDA reports)
OTITIS MEDIA CHRONIC ( 9 FDA reports)
PAIN ( 9 FDA reports)
PAIN IN JAW ( 9 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 9 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 9 FDA reports)
PLEURAL EFFUSION ( 9 FDA reports)
PLEURAL FIBROSIS ( 9 FDA reports)
PSEUDOMONAS INFECTION ( 9 FDA reports)
PULMONARY CONGESTION ( 9 FDA reports)
PULMONARY HYPERTENSION ( 9 FDA reports)
PULMONARY OEDEMA ( 9 FDA reports)
RENAL FAILURE CHRONIC ( 9 FDA reports)
RIB FRACTURE ( 9 FDA reports)
SEPTIC SHOCK ( 9 FDA reports)
SKIN ATROPHY ( 9 FDA reports)
SKIN BURNING SENSATION ( 9 FDA reports)
SOFT TISSUE DISORDER ( 9 FDA reports)
SPINAL COMPRESSION FRACTURE ( 9 FDA reports)
STREPTOCOCCAL SEPSIS ( 9 FDA reports)
SWELLING FACE ( 9 FDA reports)
THROMBOSIS IN DEVICE ( 9 FDA reports)
TONGUE ULCERATION ( 9 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 9 FDA reports)
VISUAL IMPAIRMENT ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
X-RAY ABNORMAL ( 9 FDA reports)
ANEURYSM ( 5 FDA reports)
BREAST HAEMATOMA ( 5 FDA reports)
ECCHYMOSIS ( 5 FDA reports)
KYPHOSIS ( 5 FDA reports)
PAROTITIS ( 5 FDA reports)
BACK DISORDER ( 4 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
BURSITIS ( 4 FDA reports)
NEURODERMATITIS ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
BRADYCARDIA ( 3 FDA reports)
BRONCHIECTASIS ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
PNEUMOMEDIASTINUM ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
RALES ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
FOETAL GROWTH RESTRICTION ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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