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
112706713 11270671 3 F 20130110 20160725 20150714 20160802 EXP US-TAKEDA-2015MPI004563 TAKEDA 63.45 YR F Y 89.62000 KG 20160802 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
112706713 11270671 1 PS VELCADE BORTEZOMIB 1 Subcutaneous 1.8 MG, UNK 21602 1.8 MG INJECTION
112706713 11270671 2 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral 40 MG, 1/WEEK 0 40 MG /wk
112706713 11270671 3 SS DOXIL DOXORUBICIN HYDROCHLORIDE 1 Intravenous (not otherwise specified) 59 MG, Q3WEEKS 0 59 MG Q3W
112706713 11270671 4 C ZOMETA ZOLEDRONIC ACID 1 Unknown UNK U 0
112706713 11270671 5 C KYTRIL GRANISETRON HYDROCHLORIDE 1 Unknown UNK U 0
112706713 11270671 6 C ABILIFY ARIPIPRAZOLE 1 Unknown UNK U 0
112706713 11270671 7 C PAXIL PAROXETINE HYDROCHLORIDE 1 UNK U 0
112706713 11270671 8 C PROTONIX /00661201/ OMEPRAZOLE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112706713 11270671 1 Plasma cell myeloma
112706713 11270671 2 Plasma cell myeloma
112706713 11270671 3 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
112706713 11270671 OT
112706713 11270671 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
112706713 11270671 Anaemia
112706713 11270671 Plasmacytoma
112706713 11270671 Sepsis

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
112706713 11270671 1 20121213 20130107 0
112706713 11270671 2 20121213 20130107 0
112706713 11270671 3 20121213 20130107 0