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
6736386 7396230 F 6736386-2 20100225 20100514 20100521 EXP JP-MERCK-1005USA00585 MERCK HUMAN HEALTH DIVISION 59 YR F Y 65 KG 20100521 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
6736386 1013732022 PS JANUVIA 1 ORAL 021995
6736386 1013732023 SS LIPITOR 1 ORAL
6736386 1013732024 SS GLYBURIDE 1 ORAL
6736386 1013732025 SS ACTOS 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6736386 1013732022 DIABETES MELLITUS
6736386 1013732023 HYPERCHOLESTEROLAEMIA
6736386 1013732024 DIABETES MELLITUS
6736386 1013732025 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6736386 OT

Reactions reported

Event ID PT
6736386 BLOOD PRESSURE INCREASED
6736386 PALPITATIONS
6736386 TACHYCARDIA

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
6736386 1013732022 20100223 20100225 3 DAY
6736386 1013732023 20090705 20100426 296 DAY
6736386 1013732024 20001207 20100426 3428 DAY
6736386 1013732025 20051212 20100426 1597 DAY