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

DRUG INEFFECTIVE ( 10 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
ASTHENIA ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
DIABETES MELLITUS ( 5 FDA reports)
TREMOR ( 5 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
POLLAKIURIA ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
CAROTID ARTERY OCCLUSION ( 3 FDA reports)
COMA ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
RETCHING ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACCELERATED HYPERTENSION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DIABETIC COMA ( 2 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
FEAR ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
PAIN ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 2 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MEDICATION TAMPERING ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TONGUE GEOGRAPHIC ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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