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
123389973 12338997 3 F 20160304 20160801 20160505 20160810 PER US-PFIZER INC-2016228102 PFIZER 59.00 YR M Y 0.00000 20160810 OT US US

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
123389973 12338997 1 PS RAPAMUNE SIROLIMUS 1 Oral UNK, DAILY (1-4 MG) Y 21110
123389973 12338997 2 SS RAPAMUNE SIROLIMUS 1 Oral UNK Y 21110
123389973 12338997 3 SS RAPAMUNE SIROLIMUS 1 Y 21110

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123389973 12338997 1 Heart transplant
123389973 12338997 2 Immunosuppression
123389973 12338997 3 Heart transplant

Outcome of event

Event ID CASEID OUTC COD
123389973 12338997 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123389973 12338997 Neutrophil count decreased
123389973 12338997 Product use issue
123389973 12338997 Pruritus generalised
123389973 12338997 Rash generalised
123389973 12338997 White blood cell count decreased

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
123389973 12338997 1 20151130 20160419 0
123389973 12338997 2 20160211 20160419 0