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
125663552 12566355 2 F 20160619 20160726 20160718 20160729 EXP FR-SA-2016SA129256 AVENTIS 56.00 YR A M Y 0.00000 20160729 OT FR FR

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
125663552 12566355 1 PS THYMOGLOBULINE LAPINE T-LYMPHOCYTE IMMUNE GLOBULIN 1 Intravenous (not otherwise specified) N UNK 103869
125663552 12566355 2 C DAUNORUBICIN DAUNORUBICIN 1 0
125663552 12566355 3 C ARACYTINE CYTARABINE 1 0
125663552 12566355 4 C ARACYTINE CYTARABINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125663552 12566355 1 Aplasia

Outcome of event

Event ID CASEID OUTC COD
125663552 12566355 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125663552 12566355 Acute kidney injury
125663552 12566355 Anaphylactic reaction
125663552 12566355 Disseminated intravascular coagulation
125663552 12566355 Hepatocellular injury

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
125663552 12566355 1 20160619 20160619 0
125663552 12566355 2 20160201 0
125663552 12566355 3 20160201 0
125663552 12566355 4 20160321 0