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

THROMBOCYTOPENIA ( 25 FDA reports)
HERPES ZOSTER ( 23 FDA reports)
DIARRHOEA ( 22 FDA reports)
RECTAL HAEMORRHAGE ( 22 FDA reports)
ANXIETY ( 21 FDA reports)
ATELECTASIS ( 21 FDA reports)
COMPRESSION FRACTURE ( 21 FDA reports)
PAIN ( 21 FDA reports)
PNEUMONIA ( 21 FDA reports)
PYREXIA ( 21 FDA reports)
INJURY ( 20 FDA reports)
OSTEOMYELITIS ( 20 FDA reports)
OSTEONECROSIS OF JAW ( 20 FDA reports)
CARDIOMEGALY ( 19 FDA reports)
HYPOXIA ( 19 FDA reports)
LUNG INFILTRATION ( 19 FDA reports)
MUSCULOSKELETAL PAIN ( 19 FDA reports)
HAEMATOCHEZIA ( 17 FDA reports)
HYPERTENSION ( 17 FDA reports)
RENAL FAILURE ( 17 FDA reports)
RESPIRATORY FAILURE ( 17 FDA reports)
DEPRESSION ( 16 FDA reports)
NAUSEA ( 16 FDA reports)
PLEURAL EFFUSION ( 16 FDA reports)
RENAL CYST ( 16 FDA reports)
UNRESPONSIVE TO STIMULI ( 16 FDA reports)
VOMITING ( 16 FDA reports)
ACTINIC KERATOSIS ( 15 FDA reports)
DIVERTICULUM INTESTINAL ( 15 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 15 FDA reports)
OEDEMA PERIPHERAL ( 15 FDA reports)
PULMONARY FIBROSIS ( 15 FDA reports)
ACTINOMYCOSIS ( 14 FDA reports)
ADRENAL INSUFFICIENCY ( 14 FDA reports)
ATRIAL FLUTTER ( 14 FDA reports)
BACTERAEMIA ( 14 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 14 FDA reports)
CATARACT ( 14 FDA reports)
ECCHYMOSIS ( 14 FDA reports)
FALL ( 14 FDA reports)
GASTROENTERITIS ( 14 FDA reports)
HYPOCALCAEMIA ( 14 FDA reports)
HYPOTHYROIDISM ( 14 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 14 FDA reports)
IRON DEFICIENCY ANAEMIA ( 14 FDA reports)
METABOLIC ACIDOSIS ( 14 FDA reports)
NASAL CONGESTION ( 14 FDA reports)
NECK PAIN ( 14 FDA reports)
NEPHROLITHIASIS ( 14 FDA reports)
OSTEOLYSIS ( 14 FDA reports)
PANCYTOPENIA ( 14 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 14 FDA reports)
POST HERPETIC NEURALGIA ( 14 FDA reports)
PRODUCTIVE COUGH ( 14 FDA reports)
SEPTIC SHOCK ( 14 FDA reports)
SPINAL OSTEOARTHRITIS ( 14 FDA reports)
SYNCOPE ( 14 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 14 FDA reports)
ASTHENIA ( 13 FDA reports)
BASOSQUAMOUS CARCINOMA ( 13 FDA reports)
BRAIN INJURY ( 13 FDA reports)
CIRCULATORY COLLAPSE ( 13 FDA reports)
DECREASED APPETITE ( 13 FDA reports)
HYPOACUSIS ( 13 FDA reports)
MULTIPLE MYELOMA ( 13 FDA reports)
NEOPLASM MALIGNANT ( 13 FDA reports)
TYPE 2 DIABETES MELLITUS ( 13 FDA reports)
BENIGN COLONIC NEOPLASM ( 12 FDA reports)
DYSPHAGIA ( 12 FDA reports)
GASTRITIS ( 12 FDA reports)
MENIERE'S DISEASE ( 12 FDA reports)
PAPULE ( 12 FDA reports)
DEHYDRATION ( 11 FDA reports)
DYSPNOEA ( 11 FDA reports)
FATIGUE ( 11 FDA reports)
HAEMATOMA ( 11 FDA reports)
HYPOVOLAEMIA ( 11 FDA reports)
TENDERNESS ( 11 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 10 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 10 FDA reports)
MITRAL VALVE INCOMPETENCE ( 10 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 10 FDA reports)
VENTRICULAR TACHYCARDIA ( 10 FDA reports)
BLEPHARITIS ( 9 FDA reports)
CONSTIPATION ( 9 FDA reports)
CUTIS LAXA ( 9 FDA reports)
HAEMORRHAGE ( 9 FDA reports)
OPEN ANGLE GLAUCOMA ( 9 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 9 FDA reports)
TYPE 1 DIABETES MELLITUS ( 9 FDA reports)
ANKLE FRACTURE ( 8 FDA reports)
ATRIAL FIBRILLATION ( 8 FDA reports)
MULTI-ORGAN FAILURE ( 8 FDA reports)
ANHEDONIA ( 7 FDA reports)
BARRETT'S OESOPHAGUS ( 7 FDA reports)
BONE LESION ( 7 FDA reports)
BONE NEOPLASM MALIGNANT ( 7 FDA reports)
DEEP VEIN THROMBOSIS ( 7 FDA reports)
DISCOMFORT ( 7 FDA reports)
EMOTIONAL DISTRESS ( 7 FDA reports)
FISTULA ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 7 FDA reports)
HERPES SIMPLEX ( 7 FDA reports)
HYPOPHAGIA ( 7 FDA reports)
LIFE EXPECTANCY SHORTENED ( 7 FDA reports)
LUNG NEOPLASM MALIGNANT ( 7 FDA reports)
PHYSICAL DISABILITY ( 7 FDA reports)
PROSTATE CANCER ( 7 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 7 FDA reports)
PULMONARY EMBOLISM ( 7 FDA reports)
RADICULOPATHY ( 7 FDA reports)
RECURRENT CANCER ( 7 FDA reports)
REFLUX OESOPHAGITIS ( 7 FDA reports)
SCAR ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
STEM CELL TRANSPLANT ( 7 FDA reports)
TOOTH DISORDER ( 7 FDA reports)
CELLULITIS ( 6 FDA reports)
HAEMORRHOIDS ( 6 FDA reports)
HEMIPLEGIA ( 6 FDA reports)
HIATUS HERNIA ( 6 FDA reports)
OESOPHAGEAL DILATATION ( 6 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 5 FDA reports)
BONE MARROW TRANSPLANT ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
COUGH ( 5 FDA reports)
DECUBITUS ULCER ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HAEMORRHOID OPERATION ( 5 FDA reports)
HEPATIC LESION ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
MALAISE ( 5 FDA reports)
MASS ( 5 FDA reports)
METASTASES TO BONE ( 5 FDA reports)
ORAL HERPES ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
ROTATOR CUFF SYNDROME ( 5 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 5 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
DENTAL FISTULA ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
EXPOSED BONE IN JAW ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
OPEN WOUND ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
STRESS ( 4 FDA reports)
SYMBOLIC DYSFUNCTION ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
FUNGAEMIA ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
HAEMOTHORAX ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
LEFT ATRIAL DILATATION ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
BLADDER DIVERTICULUM ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEPATIC CYST ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INFECTION ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN LESION EXCISION ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)

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