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
4869891 5908457 F 4869891-4 20000101 20051017 20051230 EXP US-MERCK-0510USA07665 MERCK HUMAN HEALTH DIVISION 74 YR M Y 109 KG 20060103 MD 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
4869891 1006777327 PS VIOXX 1 ORAL 021042
4869891 1006777328 C TRICOR 1 UNKNOWN
4869891 1006777329 C METHADONE HCL 1 UNKNOWN
4869891 1006777330 C CELEBREX 1 UNKNOWN
4869891 1006777331 C OXYCODONE 2 UNKNOWN
4869891 1006777332 C IBUPROFEN 2 UNKNOWN
4869891 1006777333 C COLCHICINE 2 UNKNOWN
4869891 1006777334 SS VIOXX 1 ORAL 021042

Indications of drugs used

Event ID DRUG SEQ INDI PT
4869891 1006777327 OSTEOARTHRITIS
4869891 1006777334 PAIN

Outcome of event

Event ID OUTC COD
4869891 DS
4869891 HO
4869891 OT

Reactions reported

Event ID PT
4869891 CEREBROVASCULAR ACCIDENT
4869891 CHEST PAIN
4869891 CHRONIC FATIGUE SYNDROME
4869891 DEEP VEIN THROMBOSIS
4869891 DEHYDRATION
4869891 DEPRESSION
4869891 DISTURBANCE IN ATTENTION
4869891 DYSPNOEA
4869891 HERNIA REPAIR
4869891 HYPOTENSION
4869891 INSOMNIA
4869891 INTERVERTEBRAL DISC PROTRUSION
4869891 LUMBAR SPINAL STENOSIS
4869891 NEUROPATHY PERIPHERAL
4869891 OEDEMA PERIPHERAL
4869891 OSTEOARTHRITIS
4869891 PAIN IN EXTREMITY
4869891 PARAPLEGIA
4869891 PULMONARY EMBOLISM
4869891 RENAL FAILURE ACUTE
4869891 SEPSIS
4869891 SUICIDAL IDEATION
4869891 URINARY TRACT INFECTION

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
4869891 1006777327 20000728 20040930 1526 DAY
4869891 1006777334 20000728 20040930 1526 DAY