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

NAUSEA ( 18 FDA reports)
RASH ( 12 FDA reports)
VOMITING ( 11 FDA reports)
FATIGUE ( 10 FDA reports)
CONJUNCTIVITIS ( 9 FDA reports)
DIARRHOEA ( 9 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
NEUROPATHY ( 5 FDA reports)
CONTUSION ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
INFECTION ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
URETHRAL HAEMORRHAGE ( 4 FDA reports)
VITAMIN K DECREASED ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
CATHETER RELATED INFECTION ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
EUPHORIC MOOD ( 3 FDA reports)
LISTLESS ( 3 FDA reports)
OSTEONECROSIS OF JAW ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
ACUTE PSYCHOSIS ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DEATH ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ACQUIRED EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COMA ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PULMONARY HYPOPLASIA ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
RENAL APLASIA ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SKULL MALFORMATION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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