The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126002703 12600270 3 F 20160726 20160727 20160804 EXP DK-TEVA-679213ISR TEVA JENSEN H, THOMSEN ST, HANSEN SS, MUNKSGAARD SB, LINDELOF M. SUPERIOR ORBITAL FISSURE SYNDROME AND OPHTHALMOPLEGIA CAUSED BY VARICELLA ZOSTER VIRUS WITH NO SKIN ERUPTION IN A PATIENT TREATED WITH TUMOR NECROSIS ALPHA INHIBITOR. CASE-REP-NEUROL 2015;7(3):221-226. 73.00 YR F Y 0.00000 20160804 OT DK DK

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126002703 12600270 1 PS MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 Unknown U 65457
126002703 12600270 2 SS infliximab INFLIXIMAB 1 Intravenous (not otherwise specified) 400MG TWO OCCASIONS 14 DAYS APART 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126002703 12600270 1 Pyoderma gangrenosum
126002703 12600270 2 Pyoderma gangrenosum

Outcome of event

Event ID CASEID OUTC COD
126002703 12600270 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126002703 12600270 Infection reactivation
126002703 12600270 Ophthalmoplegia
126002703 12600270 Orbital apex syndrome
126002703 12600270 Varicella zoster virus infection

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found