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
127177631 12717763 1 I 20160821 20160829 20160906 20160906 EXP GB-MYLANLABS-2016M1037052 MYLAN 0.00 Y 0.00000 20160906 CN GB GB

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
127177631 12717763 1 PS AZATHIOPRINE. AZATHIOPRINE 1 Unknown UNK 75568
127177631 12717763 2 SS NEORAL CYCLOSPORINE 1 Unknown 0
127177631 12717763 3 SS PREDNISOLONE. PREDNISOLONE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127177631 12717763 1 Immunosuppression
127177631 12717763 2 Immunosuppression
127177631 12717763 3 Immunosuppression

Outcome of event

Event ID CASEID OUTC COD
127177631 12717763 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127177631 12717763 Death

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

no results found

Therapies reported

no results found