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
127955081 12795508 1 I 20150916 20160929 20160929 PER CA-SEBELA IRELAND LIMITED-2016SEB00107 SEBELA 44.00 YR F Y 0.00000 20160929 OT CA CA

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
127955081 12795508 1 PS ALLOPURINOL. ALLOPURINOL 1 100 MG, DAILY Y 16084 100 MG TABLET QD
127955081 12795508 2 SS AZATHIOPRINE. AZATHIOPRINE 1 250 MG, UNK Y 0 250 MG
127955081 12795508 3 SS AZATHIOPRINE. AZATHIOPRINE 1 50 MG, UNK Y 0 50 MG
127955081 12795508 4 SS AZATHIOPRINE. AZATHIOPRINE 1 125 MG, UNK Y 0 125 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127955081 12795508 1 Product used for unknown indication
127955081 12795508 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127955081 12795508 Drug reaction with eosinophilia and systemic symptoms
127955081 12795508 Eosinophilia
127955081 12795508 Hepatic neoplasm
127955081 12795508 Pyrexia

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

no results found

Therapies reported

no results found