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

PAIN ( 9 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
ACUTE RESPIRATORY FAILURE ( 7 FDA reports)
ASTHENIA ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
BACK PAIN ( 6 FDA reports)
DEATH ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
ANHEDONIA ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
FALL ( 5 FDA reports)
GINGIVAL BLEEDING ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
METASTASES TO BONE ( 5 FDA reports)
NEOPLASM MALIGNANT ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
OSTEOARTHRITIS ( 5 FDA reports)
OSTEONECROSIS OF JAW ( 5 FDA reports)
SPINAL OSTEOARTHRITIS ( 5 FDA reports)
ABASIA ( 4 FDA reports)
ACTINIC KERATOSIS ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
MYCOSIS FUNGOIDES ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PYODERMA ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
SUNBURN ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ABSCESS ( 3 FDA reports)
ACTINOMYCOSIS ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
AREFLEXIA ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BACK DISORDER ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
COLONIC POLYP ( 3 FDA reports)
COMPRESSION FRACTURE ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
ECCHYMOSIS ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
FISTULA ( 3 FDA reports)
FOOT FRACTURE ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GINGIVAL EROSION ( 3 FDA reports)
GINGIVAL SWELLING ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HYPERLIPIDAEMIA ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
IRRITABLE BOWEL SYNDROME ( 3 FDA reports)
JOINT EFFUSION ( 3 FDA reports)
LDL/HDL RATIO INCREASED ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
MENISCUS LESION ( 3 FDA reports)
METASTASES TO LUNG ( 3 FDA reports)
METASTASES TO SPINE ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
OPEN WOUND ( 3 FDA reports)
ORAL CAVITY FISTULA ( 3 FDA reports)
ORAL DISORDER ( 3 FDA reports)
ORAL INFECTION ( 3 FDA reports)
ORAL PAIN ( 3 FDA reports)
OROPHARYNGEAL BLISTERING ( 3 FDA reports)
OSTEOMYELITIS ACUTE ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PERIODONTAL DISEASE ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
PURULENT DISCHARGE ( 3 FDA reports)
RADICULOPATHY ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
SALIVARY GLAND MASS ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SPINAL COLUMN STENOSIS ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLADDER NECROSIS ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 2 FDA reports)
CORNEAL THINNING ( 2 FDA reports)
DIABETIC COMPLICATION ( 2 FDA reports)
DIABETIC EYE DISEASE ( 2 FDA reports)
ENTEROBACTER TEST POSITIVE ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYDROURETER ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
INJURY ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
PHYSICAL DISABILITY ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
SEBORRHOEIC KERATOSIS ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
ULCER ( 2 FDA reports)
URETERIC DILATATION ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANGER ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMA ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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