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
6138276 6956715 I 6138276-5 20081111 20090327 20090331 EXP B0567640A GLAXOSMITHKLINE 49 YR F Y 20090331 CN FRANCE

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
6138276 1011356976 PS NABUCOX 2 ORAL 1.5TAB PER DAY 19583
6138276 1011356977 SS REMICADE 1 INTRAVENOUS
6138276 1011356978 SS NEXIUM 1 ORAL 40MG FOUR TIMES PER DAY
6138276 1011356979 C CRESTOR 1 ORAL 10MG FOUR TIMES PER DAY
6138276 1011356980 C MALARONE 1
6138276 1011356981 C CLONAZEPAM 1
6138276 1011356982 C SKENAN 2 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6138276 1011356976 ANKYLOSING SPONDYLITIS
6138276 1011356977 ANKYLOSING SPONDYLITIS
6138276 1011356980 MALARIA PROPHYLAXIS

Outcome of event

Event ID OUTC COD
6138276 HO

Reactions reported

Event ID PT
6138276 BLOOD AMYLASE INCREASED
6138276 DERMATITIS
6138276 ECZEMA
6138276 PRURIGO
6138276 PRURITUS GENERALISED
6138276 SKIN REACTION

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
6138276 1011356976 20060101
6138276 1011356977 20050201
6138276 1011356978 20060101
6138276 1011356979 20080101 20090201 1 YR
6138276 1011356980 19990101
6138276 1011356981 19990101
6138276 1011356982 19990101