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
110909428 11090942 8 F 20150424 20160909 20150505 20160912 EXP DE-PFIZER INC-2015150324 PFIZER 66.00 YR M Y 78.00000 KG 20160912 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
110909428 11090942 1 PS TEMSIROLIMUS TEMSIROLIMUS 1 25 MG, CYCLE 3 N 22088 25 MG CONCENTRATE FOR SOLUTION FOR INFUSION
110909428 11090942 2 SS RITUXIMAB RITUXIMAB 1 750 MG, UNK U 0 750 MG
110909428 11090942 3 SS DEXAMETHASONE. DEXAMETHASONE 1 40 MG, UNK U 0 40 MG
110909428 11090942 4 SS CISPLATIN. CISPLATIN 1 200 MG, UNK U 0 200 MG
110909428 11090942 5 SS CYTARABINE. CYTARABINE 1 8000 MG, UNK U 0 8000 MG
110909428 11090942 6 C NEULASTA PEGFILGRASTIM 1 AFTER EACH CYCLE 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
110909428 11090942 LT
110909428 11090942 DE
110909428 11090942 HO
110909428 11090942 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
110909428 11090942 Neutropenic sepsis
110909428 11090942 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
110909428 11090942 1 20150206 20150421 0
110909428 11090942 2 20150207 20150415 0
110909428 11090942 3 20150209 20150419 0
110909428 11090942 4 20150208 20150416 0
110909428 11090942 5 20150209 20150417 0