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

DYSPNOEA ( 9 FDA reports)
VOMITING ( 8 FDA reports)
CONVULSION ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
ASTHENIA ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
CHOLESTASIS ( 6 FDA reports)
HEPATITIS ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
DISORIENTATION ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
HALLUCINATION, VISUAL ( 5 FDA reports)
AFFECTIVE DISORDER ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
APHASIA ( 4 FDA reports)
APRAXIA ( 4 FDA reports)
BLINDNESS ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 4 FDA reports)
CSF PROTEIN ABNORMAL ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
JC VIRUS INFECTION ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
NEUROLOGIC NEGLECT SYNDROME ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 4 FDA reports)
PERSONALITY CHANGE ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
COMA ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FIXED ERUPTION ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
MALAISE ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CITROBACTER INFECTION ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PENIS DISORDER ( 2 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RETINOPATHY HYPERTENSIVE ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TRICHORRHEXIS ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VITREOUS FLOATERS ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALLERGY TEST POSITIVE ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
CORNEAL DYSTROPHY ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
DECEREBRATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FALL ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS E ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
URINE ARSENIC INCREASED ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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