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
6682902 7328918 F 6682902-9 20100311 20100408 20100415 EXP B0640107A GLAXOSMITHKLINE 71 YR M Y 20100415 MD JAPAN

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
6682902 1013508560 PS AVOLVE 2 ORAL .5MG PER DAY 21319
6682902 1013508561 SS CRESTOR 1 ORAL
6682902 1013508562 SS ATELEC 2 ORAL
6682902 1013508563 SS ACTOS 1
6682902 1013508564 SS ETHYL ICOSAPENTATE 2
6682902 1013508565 SS FLIVAS 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6682902 1013508560 DRUG USE FOR UNKNOWN INDICATION
6682902 1013508561 DRUG USE FOR UNKNOWN INDICATION
6682902 1013508562 DRUG USE FOR UNKNOWN INDICATION
6682902 1013508563 DRUG USE FOR UNKNOWN INDICATION
6682902 1013508564 DRUG USE FOR UNKNOWN INDICATION
6682902 1013508565 DRUG USE FOR UNKNOWN INDICATION

Outcome of event

Event ID OUTC COD
6682902 OT

Reactions reported

Event ID PT
6682902 ALANINE AMINOTRANSFERASE ABNORMAL
6682902 ASPARTATE AMINOTRANSFERASE ABNORMAL
6682902 BLOOD AMYLASE
6682902 HEPATIC FUNCTION ABNORMAL
6682902 LOW DENSITY LIPOPROTEIN ABNORMAL
6682902 NASOPHARYNGITIS
6682902 OROPHARYNGEAL DISCOMFORT
6682902 SENSORY DISTURBANCE

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
6682902 1013508560 20100303 20100311 1 WK