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
112326023 11232602 3 F 20150424 20160830 20150701 20160909 EXP DE-TEVA-574588GER TEVA 66.00 YR M Y 78.00000 KG 20160909 MD DE DE

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
112326023 11232602 1 PS CISPLATIN. CISPLATIN 1 Unknown LAST DOSE PRIOR TO AE 16-APR-2015 U 74656 200 MG
112326023 11232602 2 SS DEXAMETHASONE. DEXAMETHASONE 1 Unknown LAST DOSE PRIOR TO AE 19-APR-2015 U 85456 40 MG
112326023 11232602 3 SS Temsirolimus TEMSIROLIMUS 1 Unknown CYCLE 3; LAST DOSE PRIOR TO AE 21-APR-2015 N 0 25 MG SOLUTION FOR INFUSION
112326023 11232602 4 SS Rituximab RITUXIMAB 1 Unknown LAST DOSE PRIOR TO AE 15-APR-2015 U 0 750 MG
112326023 11232602 5 SS CYTARABINE. CYTARABINE 1 Unknown LAST DOSE PRIOR TO AE 17-APR-2015 U 0 8000 MG
112326023 11232602 6 C NEULASTA PEGFILGRASTIM 1 AFTER EACH CYCLE 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
112326023 11232602 LT
112326023 11232602 HO
112326023 11232602 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
112326023 11232602 Neutropenic sepsis
112326023 11232602 Thrombocytopenia

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
112326023 11232602 1 20150208 20150416 0
112326023 11232602 2 20150209 20150419 0
112326023 11232602 3 20150206 20150421 0
112326023 11232602 4 20150207 20150415 0
112326023 11232602 5 20150209 20150417 0
112326023 11232602 6 20150420 20150420 0