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
6700501 7023260 F 6700501-7 20100423 20100428 EXP A0790535A GLAXOSMITHKLINE 59 YR F Y 97.7 KG 20100428 OT 20070217 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
6700501 1013585019 PS AVANDIA 1 ORAL 4MG TWICE PER DAY 021071
6700501 1013585020 C GLUCOPHAGE 1
6700501 1013585021 C XOPENEX 1
6700501 1013585022 C ATENOLOL 1
6700501 1013585023 C LEVOTHROID 1
6700501 1013585024 C ACCUPRIL 1
6700501 1013585025 C LIPITOR 1
6700501 1013585026 C GLUCOTROL 1
6700501 1013585027 C PAXIL 1
6700501 1013585028 C NEURONTIN 1
6700501 1013585029 C TOPROL-XL 1
6700501 1013585030 C PRILOSEC 1
6700501 1013585031 C LANTUS 1
6700501 1013585032 C DUONEB 1

Indications of drugs used

no results found

Outcome of event

Event ID OUTC COD
6700501 DE
6700501 HO

Reactions reported

Event ID PT
6700501 ARRHYTHMIA
6700501 ATRIAL FIBRILLATION
6700501 CARDIAC FAILURE CONGESTIVE
6700501 CORONARY ARTERY OCCLUSION

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
6700501 1013585019 20020201 20070124