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

ASTHMA ( 9 FDA reports)
SINUSITIS ( 9 FDA reports)
STAPHYLOCOCCAL INFECTION ( 9 FDA reports)
DRUG RESISTANCE ( 7 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 7 FDA reports)
DYSPHONIA ( 7 FDA reports)
CATHETER RELATED COMPLICATION ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
DRUG EFFECT DECREASED ( 6 FDA reports)
DISEASE RECURRENCE ( 5 FDA reports)
EOSINOPHILIA ( 5 FDA reports)
HYPOXIA ( 5 FDA reports)
INFLUENZA LIKE ILLNESS ( 5 FDA reports)
JUGULAR VEIN THROMBOSIS ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
RASH PUSTULAR ( 5 FDA reports)
RHINITIS ALLERGIC ( 5 FDA reports)
BRADYCARDIA ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
FALL ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
PATHOGEN RESISTANCE ( 3 FDA reports)
RHINITIS ( 3 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
CATHETER SITE INFLAMMATION ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
RASH ( 2 FDA reports)
REACTION TO AZO-DYES ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
URTICARIA PHYSICAL ( 2 FDA reports)
URTICARIA THERMAL ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
IMPLANT SITE THROMBOSIS ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUPUS ENDOCARDITIS ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYCOTIC ALLERGY ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
OCCUPATIONAL EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RADIOALLERGOSORBENT TEST POSITIVE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
SALIVARY GLAND ADENOMA ( 1 FDA reports)
SCAR ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VITRITIS ( 1 FDA reports)

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