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

DRUG INTERACTION ( 7 FDA reports)
FATIGUE ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
COUGH ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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