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
6699441 7368202 I 6699441-1 20100414 20100419 20100427 EXP JP-MERCK-1004USA03882 MERCK HUMAN HEALTH DIVISION 70 YR F Y 20100428 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
6699441 1013580834 PS JANUVIA 1 ORAL
6699441 1013580835 SS AMARYL 1 ORAL
6699441 1013580836 SS ACTOS 1 ORAL
6699441 1013580837 SS LASIX 1 ORAL
6699441 1013580838 C UNASYN 1 INTRAVENOUS
6699441 1013580839 C THEODRIP 2 INTRAVENOUS

Indications of drugs used

Event ID DRUG SEQ INDI PT
6699441 1013580834 DIABETES MELLITUS
6699441 1013580835 DIABETES MELLITUS
6699441 1013580836 DIABETES MELLITUS
6699441 1013580837 OEDEMA
6699441 1013580838 PNEUMONIA
6699441 1013580839 PNEUMONIA

Outcome of event

Event ID OUTC COD
6699441 LT

Reactions reported

Event ID PT
6699441 CARDIAC FAILURE

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
6699441 1013580834 20100407 20100414 8 DAY
6699441 1013580835 20010606
6699441 1013580836 20010606
6699441 1013580837 20061117