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

DYSPNOEA ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
AGITATION ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 2 FDA reports)
RASH ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
TRANCE ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD LUTEINISING HORMONE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COMA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FALL ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERPROLACTINAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
OROPHARYNGEAL PLAQUE ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TRANSFERRIN DECREASED ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITAMIN K DEFICIENCY ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)

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