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
4960040 5951426 F 4960040-0 20020721 20051215 20060331 EXP US-MERCK-0512USA02526 MERCK HUMAN HEALTH DIVISION 47 YR M Y 113 KG 20060403 LW 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
4960040 1007119013 PS VIOXX 1 ORAL 21042
4960040 1007119014 C CELEBREX 1 UNKNOWN
4960040 1007119015 C VICODIN 1 UNKNOWN
4960040 1007119016 C FLEXERIL 1 UNKNOWN
4960040 1007119017 C ULTRAM 1 UNKNOWN
4960040 1007119018 C LIPITOR 1 UNKNOWN
4960040 1007119019 C DIOVAN 1 UNKNOWN

Indications of drugs used

Event ID DRUG SEQ INDI PT
4960040 1007119013 BACK PAIN
4960040 1007119014 ARTHRITIS
4960040 1007119015 BACK PAIN
4960040 1007119016 PAIN
4960040 1007119017 BACK PAIN
4960040 1007119018 BLOOD CHOLESTEROL INCREASED
4960040 1007119019 HYPERTENSION

Outcome of event

Event ID OUTC COD
4960040 HO

Reactions reported

Event ID PT
4960040 MYOCARDIAL INFARCTION
4960040 MYOCARDIAL ISCHAEMIA
4960040 OVERDOSE
4960040 SKIN LACERATION

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
4960040 1007119013 20020721 20021116 119 DAY
4960040 1007119014 20020709 20021116 131 DAY
4960040 1007119015 20021010 20021116 38 DAY
4960040 1007119016 20021021 20021116 27 DAY
4960040 1007119017 20020722 20021116 118 DAY
4960040 1007119018 20021010
4960040 1007119019 20021010