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
121823092 12182309 2 F 20151203 20160726 20160316 20160728 EXP FR-ROCHE-1724886 ROCHE 0.00 M Y 66.00000 KG 20160728 MD FR FR

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
121823092 12182309 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) DATE OF LAST DOSE PRIOR TO SAE WAS ON: 12/NOV/2015 (525 MG) Y 125085 SOLUTION FOR INFUSION
121823092 12182309 2 SS CARBOPLATINE CARBOPLATIN 1 Intravenous (not otherwise specified) DATE OF LAST DOSE PRIOR TO SAE WAS ON: 22/OCT/2015 (464 MG) U 0
121823092 12182309 3 SS ALIMTA PEMETREXED DISODIUM 1 Intravenous (not otherwise specified) DATE OF LAST DOSE PRIOR TO SAE WAS ON: 22/OCT/2015 (960) Y 0
121823092 12182309 4 SS BISOPROLOL BISOPROLOL 1 Oral Y 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121823092 12182309 1 Ovarian cancer
121823092 12182309 2 Ovarian cancer
121823092 12182309 3 Ovarian cancer
121823092 12182309 4 Hypertension

Outcome of event

Event ID CASEID OUTC COD
121823092 12182309 HO
121823092 12182309 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121823092 12182309 Confusional state
121823092 12182309 General physical health deterioration
121823092 12182309 Hypotension

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
121823092 12182309 1 20150910 0
121823092 12182309 2 20150820 0
121823092 12182309 3 20150820 0
121823092 12182309 4 20100123 20151230 0