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

TREMOR ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
PULMONARY TOXICITY ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
COMA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
FALL ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)

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