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

NAUSEA ( 7 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 6 FDA reports)
ASTHENIA ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
SKIN FLAP NECROSIS ( 4 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
SCOLIOSIS ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
CHOLECYSTITIS INFECTIVE ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CYST ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY THROMBOSIS ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHOSPASM PARADOXICAL ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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