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

OEDEMA PERIPHERAL ( 9 FDA reports)
DYSPNOEA ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
ASTHMA ( 3 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
JUGULAR VEIN DISTENSION ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NARCOLEPSY ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPLICATION SITE HAEMATOMA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COMA ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DUODENECTOMY ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FALL ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 1 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INJECTION SITE DESQUAMATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RHINOVIRUS INFECTION ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SMALL INTESTINE OPERATION ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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