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
6677449 6962547 F 6677449-X 20100409 20100412 EXP A0777158A GLAXOSMITHKLINE 67 YR F Y 50.9 KG 20100412 OT 20070604 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
6677449 1013485040 PS AVANDIA 1 ORAL 2MG PER DAY 021071
6677449 1013485041 C LOPRESSOR 1
6677449 1013485042 C FOSAMAX 1
6677449 1013485043 C PROCARDIA XL 1
6677449 1013485044 C ASPIRIN 1 81MG PER DAY
6677449 1013485045 C ZOLOFT 1
6677449 1013485046 C VASOTEC 1
6677449 1013485047 C HYDREA 1
6677449 1013485048 C GLIPIZIDE 1
6677449 1013485049 C CALCIUM 2
6677449 1013485050 C MULTI-VITAMIN 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6677449 1013485040 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6677449 DE
6677449 HO

Reactions reported

Event ID PT
6677449 ATRIAL FIBRILLATION
6677449 CARDIAC FAILURE CONGESTIVE
6677449 CARDIOMYOPATHY
6677449 CORONARY ARTERY DISEASE
6677449 CORONARY ARTERY INSUFFICIENCY
6677449 HYPERTENSION
6677449 MYOCARDIAL INFARCTION
6677449 NERVOUS SYSTEM DISORDER

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
6677449 1013485040 20030801 20070524