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
123714732 12371473 2 F 20160823 20160516 20160906 EXP US-ROCHE-1756698 ROCHE 62.00 YR M Y 72.60000 KG 20160906 MD 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
123714732 12371473 1 PS Bevacizumab BEVACIZUMAB 1 Unknown 125085
123714732 12371473 2 SS IPILIMUMAB IPILIMUMAB 1 Unknown 0 224 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123714732 12371473 1 Malignant melanoma
123714732 12371473 2 Malignant melanoma

Outcome of event

Event ID CASEID OUTC COD
123714732 12371473 OT
123714732 12371473 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
123714732 12371473 Acute respiratory distress syndrome
123714732 12371473 Death
123714732 12371473 Dyspnoea

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
123714732 12371473 2 20150730 0