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VITRITIS ( 7 FDA reports)
OFF LABEL USE ( 7 FDA reports)
HYPOPYON ( 7 FDA reports)
CORNEAL OEDEMA ( 7 FDA reports)
ENDOPHTHALMITIS ( 7 FDA reports)
ANTERIOR CHAMBER FIBRIN ( 5 FDA reports)
INFUSION RELATED REACTION ( 5 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
LIP OEDEMA ( 3 FDA reports)
LIVER INJURY ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
RASH ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
TRYPTASE DECREASED ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)

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