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
6671475 7347580 I 6671475-2 20100329 20100330 20100407 EXP JP-MERCK-1004USA00141 MERCK HUMAN HEALTH DIVISION 84 YR M Y 20100407 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
6671475 1013460186 PS JANUVIA 1 ORAL 21995
6671475 1013460187 SS ASPIRIN 1 ORAL
6671475 1013460188 SS PROTECADIN 2 ORAL
6671475 1013460189 SS ACTOS 1 ORAL
6671475 1013460190 SS AMARYL 1 ORAL
6671475 1013460191 SS LIVALO 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6671475 1013460186 HYPERGLYCAEMIA
6671475 1013460187 THROMBOSIS PROPHYLAXIS
6671475 1013460189 HYPERGLYCAEMIA
6671475 1013460190 HYPERGLYCAEMIA
6671475 1013460191 HYPERLIPIDAEMIA

Outcome of event

Event ID OUTC COD
6671475 HO
6671475 LT

Reactions reported

Event ID PT
6671475 MYOCARDIAL INFARCTION

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
6671475 1013460186 20100121
6671475 1013460187 20081211
6671475 1013460188 20081211
6671475 1013460189 20081211
6671475 1013460190 20081211
6671475 1013460191 20081211