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

PRURITUS ( 6 FDA reports)
RASH ( 5 FDA reports)
CANDIDIASIS ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
ANEURYSM ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
COUGH ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEPATIC VEIN THROMBOSIS ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
RHINITIS ALLERGIC ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
ANXIETY ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTRAOCULAR LENS IMPLANT ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POLYP ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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