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
5005209 6055728 I 5005209-4 20050517 20060509 20060512 EXP HQWYE817920MAY05 WYETH PHARMACEUTICALS INC. 75 YR F N 49.49 KG 20060511 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
5005209 1007299201 SS TEMSIROLIMUS (TEMSIROLIMUS) 2 ORAL 30 MG ONCE DAILY; DAYS 1 -5 (14 DAY CYCLE), ORAL D D 2004P0919
5005209 1007324483 PS LETROZOLE 2 ORAL 2.5 MG 1X PER 1 DAY, ORAL D D
5005209 1007324484 C SYNTHROID 1
5005209 1007324485 C ZOCOR 1
5005209 1007324486 C LISINOPRIL 1
5005209 1007324487 C METOPROLOL SUCCINATE 1
5005209 1007324488 C PRANDIN 1
5005209 1007324489 C NORVASC 1
5005209 1007324490 C ASPIRIN 1
5005209 1007324491 C ACETAMINOPHEN 1
5005209 1007324492 C COLACE (DOCUSATE SODIUM) 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
5005209 1007299201 BREAST CANCER METASTATIC
5005209 1007324483 BREAST CANCER METASTATIC

Outcome of event

Event ID OUTC COD
5005209 HO
5005209 LT
5005209 OT

Reactions reported

Event ID PT
5005209 ANGIONEUROTIC OEDEMA

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

Event ID RPSR COD
5005209 SDY

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5005209 1007299201 20050328 20050514
5005209 1007324483 20050328 20050514