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
6696850 7366221 F 6696850-1 20090501 20100420 20100426 EXP US-MERCK-0910USA03017 MERCK HUMAN HEALTH DIVISION 86 YR M Y 70 KG 20100426 MD 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
6696850 1013568997 PS JANUVIA 1 ORAL 021995
6696850 1013568998 C INSULIN 2 UNKNOWN
6696850 1013568999 SS ACTOS 1 ORAL
6696850 1013569000 C STARLIX 1 ORAL
6696850 1013569001 C EXFORGE 1 ORAL
6696850 1013569002 C PREDNISONE 2 UNKNOWN

Indications of drugs used

Event ID DRUG SEQ INDI PT
6696850 1013568997 TYPE 2 DIABETES MELLITUS
6696850 1013568999 TYPE 2 DIABETES MELLITUS
6696850 1013569000 TYPE 2 DIABETES MELLITUS
6696850 1013569002 DERMATITIS

Outcome of event

Event ID OUTC COD
6696850 DS
6696850 LT
6696850 OT

Reactions reported

Event ID PT
6696850 IMPAIRED GASTRIC EMPTYING
6696850 PANCREATITIS

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
6696850 1013568997 20060101 20090101
6696850 1013568999 20000101
6696850 1013569000 20000101
6696850 1013569001 20080101
6696850 1013569002 20060101