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
6720409 7387637 I 6720409-0 20100329 20100430 20100506 EXP WAES 1004USA04801 MERCK + CO., INC. 78 YR M N 20100505 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
6720409 1013666299 PS JANUVIA 1 ORAL 25 MG/DAILY, PO D D 21995
6720409 1013685097 SS AMARYL 1 ORAL 2 MG/DAILY, PO U U
6720409 1013685099 SS ACTOS 1 ORAL 15 MG/DAILY, PO U U
6720409 1013685100 C ASPIRIN 1
6720409 1013685101 C PANALDINE 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6720409 1013666299 DIABETES MELLITUS
6720409 1013685097 DIABETES MELLITUS
6720409 1013685099 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6720409 HO
6720409 LT

Reactions reported

Event ID PT
6720409 HYPOGLYCAEMIA

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

Event ID RPSR COD
6720409 FGN
6720409 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6720409 1013666299 20100424