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
127291681 12729168 1 I 20160628 0 20160908 20160908 DIR US-FDA-350100 FDA-CTU 63.00 YR F N 64.80000 KG 20160908 Y PH 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
127291681 12729168 1 PS OXALIPLATIN. OXALIPLATIN 1 Intravenous drip OTHER Y D OX11507A 20170228 0 150 MG
127291681 12729168 3 C EMEND APREPITANT 1 0
127291681 12729168 5 C ALOXI PALONOSETRON HYDROCHLORIDE 1 0
127291681 12729168 7 C DECADRON DEXAMETHASONE 1 0
127291681 12729168 9 C LEUCOVORIN. LEUCOVORIN 1 0
127291681 12729168 11 C FLUOROURACIL. FLUOROURACIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127291681 12729168 1 Rectal cancer

Outcome of event

Event ID CASEID OUTC COD
127291681 12729168 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127291681 12729168 Dyspnoea
127291681 12729168 Hypoaesthesia
127291681 12729168 Stridor
127291681 12729168 Wheezing

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID CASEID RPSR COD
127291681 12729168 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127291681 12729168 1 2 HR