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

SEPSIS ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 3 FDA reports)
VASCULITIS ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 1 FDA reports)
CHILLS ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)

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