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

ASTHENIA ( 11 FDA reports)
VOMITING ( 9 FDA reports)
COMA ( 8 FDA reports)
NAUSEA ( 8 FDA reports)
PRURITUS ( 7 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
ENCEPHALOPATHY ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
FATIGUE ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
ALOPECIA ( 3 FDA reports)
APHASIA ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
POISONING ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WHITE BLOOD CELLS STOOL POSITIVE ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ADAMS-STOKES SYNDROME ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BLASTOCYSTIS INFECTION ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYST ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
ECHINOCOCCIASIS ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ERYTHROSIS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL OEDEMA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC CALCIFICATION ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ECHINOCOCCIASIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MAZZOTTI REACTION ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NODULE ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PARASITIC INFECTION INTESTINAL ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL HYPOPLASIA ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCHISTOSOMA TEST POSITIVE ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS POLYP ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOXOCARIASIS ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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