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
6685297 7348890 F 6685297-X 20100322 20100412 20100416 EXP JP-MERCK-1004USA00546 MERCK HUMAN HEALTH DIVISION 78 YR M Y 20100419 MD 20100324 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
6685297 1013520858 PS JANUVIA 1 ORAL
6685297 1013520859 SS AMARYL 1 ORAL
6685297 1013520860 SS AMARYL 1 ORAL
6685297 1013520861 SS ACTOS 1 ORAL
6685297 1013520862 C LEUPROLIDE ACETATE 2 SUBCUTANEOUS

Indications of drugs used

Event ID DRUG SEQ INDI PT
6685297 1013520858 DIABETES MELLITUS
6685297 1013520859 DIABETES MELLITUS
6685297 1013520861 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6685297 DE
6685297 HO

Reactions reported

Event ID PT
6685297 HYPOGLYCAEMIA
6685297 PNEUMONIA

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
6685297 1013520858 20100106 20100322 76 DAY
6685297 1013520859 20091125 20100322 118 DAY
6685297 1013520860 20061017 20091124 1135 DAY
6685297 1013520861 20051001 20100322
6685297 1013520862 20100301