The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
4832350 5892321 F 2 4832350-9 20051107 20051117 EXP USA0509107641 ELI LILLY AND COMPANY 78 YR F N 68 KG 20051109 MD 20050830 UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
4832350 1006642248 PS ALIMTA 1 500 MG 21462
4832350 1006665621 C VITAMIN B-12 1
4832350 1006665622 C FOLIC ACID 1
4832350 1006665623 C CORTICOSTEROID NOS 2
4832350 1006665624 C CISPLATIN 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
4832350 1006642248 NON-SMALL CELL LUNG CANCER METASTATIC

Outcome of event

Event ID OUTC COD
4832350 DE
4832350 HO
4832350 OT

Reactions reported

Event ID PT
4832350 CONDITION AGGRAVATED
4832350 GASTROINTESTINAL HAEMORRHAGE
4832350 HAEMATOCRIT DECREASED
4832350 HAEMOGLOBIN DECREASED
4832350 PLATELET COUNT INCREASED

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

Event ID RPSR COD
4832350 CR
4832350 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4832350 1006642248 20050425 20050808