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ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
HEPATITIS B ( 6 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
COUGH ( 4 FDA reports)
MYOPATHY ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
VOMITING ( 4 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
MUSCLE SWELLING ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
GLOBULINS DECREASED ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATITIS B VIRUS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
STILLBIRTH ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS B DNA INCREASED ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TETANY ( 1 FDA reports)

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