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
4623943 5759607 F 4623943-2 20020101 20050308 20050331 EXP US-MERCK-0503USA01265 MERCK HUMAN HEALTH DIVISION M Y 20050331 OT

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
4623943 1005834856 PS VIOXX 1 ORAL 21042
4623943 1005834857 C ASPIRIN 1 UNKNOWN
4623943 1005834858 C LISINOPRIL 2 UNKNOWN

Indications of drugs used

Event ID DRUG SEQ INDI PT
4623943 1005834857 CARDIAC DISORDER
4623943 1005834858 CARDIAC DISORDER

Outcome of event

Event ID OUTC COD
4623943 HO

Reactions reported

Event ID PT
4623943 ANGINA PECTORIS
4623943 ASTHENIA
4623943 CHEST PAIN
4623943 DIZZINESS
4623943 HEAT STROKE
4623943 LOSS OF CONSCIOUSNESS
4623943 MALAISE
4623943 NAUSEA
4623943 URINARY TRACT DISORDER
4623943 VOMITING

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
4623943 1005834856 20020501 20040101