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
4974812 6045621 I 4974812-X 20030912 20041022 20060216 PER 2004IM000500 INTERMUNE 53 YR F N 67.5 KG 20060214 MD CANADA

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
4974812 1007177154 PS INTERFERON GAMMA-1B 2 SUBCUTANEOUS 100 UG, TIW, SUBCUTANEOUS D D
4974812 1007285188 SS CARBOPLATIN 1 INTRAVENOUS 653 MG, Q3W, INTRAVENOUS D D
4974812 1007285210 SS PACLITAXEL 1 INTRAVENOUS 306 MG, Q3W, INTRAVENOUS D D
4974812 1007285211 C RANITIDINE 1
4974812 1007285213 C VITAMIN B6 1
4974812 1007285290 C WB3 LINOLINIC ACID 2
4974812 1007285291 C TYLENOL (CAPLET) 1
4974812 1007285292 C SENOKOT 1
4974812 1007285293 C IMOVANE 2
4974812 1007285294 C LASIX 1
4974812 1007285295 C SPIRONOLACTONE 1
4974812 1007285297 C ECHINCEA 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
4974812 1007177154 OVARIAN CANCER
4974812 1007285188 OVARIAN CANCER
4974812 1007285210 OVARIAN CANCER

Outcome of event

Event ID OUTC COD
4974812 OT

Reactions reported

Event ID PT
4974812 NEUTROPENIA

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

Event ID RPSR COD
4974812 FGN
4974812 HP
4974812 SDY

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4974812 1007177154 20030424 20030911
4974812 1007285188 20030424 20030903
4974812 1007285210 20030424 20030903