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
7299474 7628157 F 7299474-0 20061110 20110204 20110217 EXP A0614327E GLAXOSMITHKLINE 59 YR F Y 72.8 KG 20110217 MD IRELAND

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
7299474 1015808090 SS DOCETAXEL 1 INTRAVENOUS 100MGM2 CYCLIC
7299474 1015808095 C VALOID 2 ORAL 50MG THREE TIMES PER DAY
7299474 1015808097 C ZOFRAN 1 ORAL 8MG TWICE PER DAY
7299474 1015808094 C CODEINE LINCTUS 2 ORAL 10MG AS REQUIRED
7299474 1015808099 C SENOKOT 1 ORAL 2TAB PER DAY
7299474 1015808089 PS LAPATINIB 2 ORAL 500MG PER DAY 022059
7299474 1015808096 C LACRILUBE 2 OPHTHALMIC 3DROP AS REQUIRED
7299474 1015808098 C LACTULOSE 1 ORAL 30ML PER DAY
7299474 1015808093 C CIPROXIN 2 INTRAVENOUS 800MG PER DAY
7299474 1015808101 C CHLOROMYCETIN 1 OPHTHALMIC
7299474 1015808092 C KLACID 2 1G PER DAY
7299474 1015808091 SS TRASTUZUMAB 2 INTRAVENOUS 4MGK WEEKLY
7299474 1015808100 C SLOW-K 1 ORAL 2TAB PER DAY

Indications of drugs used

no results found

Outcome of event

Event ID OUTC COD
7299474 OT

Reactions reported

Event ID PT
7299474 NEUTROPENIA

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
7299474 1015808090 20060720
7299474 1015808089 20060720
7299474 1015808091 20060720