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
124852432 12485243 2 F 20140722 20160624 20160621 20160705 EXP CN-TAKEDA-2016MPI005673 TAKEDA 64.26 YR M Y 44.00000 KG 20160705 CN CN CN

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
124852432 12485243 1 PS VELCADE BORTEZOMIB 1 Intravenous (not otherwise specified) 1.3 MG/M2, UNK 21602 1.3 MG/M**2 INJECTION
124852432 12485243 2 SS VELCADE BORTEZOMIB 1 Intravenous (not otherwise specified) 1.3 MG/M2, UNK 21602 1.3 MG/M**2 INJECTION
124852432 12485243 3 SS VELCADE BORTEZOMIB 1 Subcutaneous 1.3 MG/M2, UNK 21602 1.3 MG/M**2 INJECTION
124852432 12485243 4 SS VELCADE BORTEZOMIB 1 Subcutaneous 1.3 MG/M2, UNK 21602 1.3 MG/M**2 INJECTION
124852432 12485243 5 C DOXORUBICIN /00330902/ DOXORUBICIN 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124852432 12485243 1 Mantle cell lymphoma
124852432 12485243 2 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
124852432 12485243 OT
124852432 12485243 HO
124852432 12485243 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
124852432 12485243 Bone marrow failure
124852432 12485243 Disease progression
124852432 12485243 Gastrointestinal infection
124852432 12485243 Lung infection
124852432 12485243 Pneumonia

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
124852432 12485243 1 20140721 0
124852432 12485243 2 20140721 0
124852432 12485243 3 20140721 0
124852432 12485243 4 20140721 0