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
124772112 12477211 2 F 20160802 20160617 20160816 EXP GB-WATSON-2016-12616 WATSON 52.00 YR M Y 0.00000 20160816 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
124772112 12477211 1 SS AZATHIOPRINE. AZATHIOPRINE 1 Unknown 25 MG, UNKNOWN U UNCONFIRMED 0 25 MG TABLET
124772112 12477211 2 SS AZATHIOPRINE. AZATHIOPRINE 1 Unknown 50 MG, UNKNOWN U UNCONFIRMED 0 50 MG TABLET
124772112 12477211 3 PS PREDNISOLONE. PREDNISOLONE 1 Unknown 5 MG, UNKNOWN U UNCONFIRMED 80354 5 MG TABLET
124772112 12477211 4 SS ADOPORT TACROLIMUS 1 Unknown 1 MG, UNKNOWN U 0 1 MG
124772112 12477211 5 SS ADOPORT TACROLIMUS 1 Unknown 0.5 MG, UNK U 0 .5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124772112 12477211 1 Immunosuppression
124772112 12477211 3 Immunosuppression
124772112 12477211 4 Immunosuppression

Outcome of event

Event ID CASEID OUTC COD
124772112 12477211 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124772112 12477211 Abdominal pain
124772112 12477211 Malaise

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

no results found

Therapies reported

no results found