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
4387948 4149888 F 4387948-1 19990101 20030407 20040630 EXP US-MERCK-0304USA00752 MERCK HUMAN HEALTH DIVISION 59 YR M Y 100 KG 20040701 MD

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
4387948 1004981114 C LITHIUM CARBONATE 1 UNKNOWN
4387948 1004981115 PS VIOXX 1 ORAL
4387948 1004981116 SS VIOXX 1 ORAL
4387948 1004981117 SS VIOXX 1 ORAL
4387948 1004981118 SS VIOXX 1 ORAL
4387948 1004981119 SS VIOXX 1 ORAL
4387948 1004981120 SS VIOXX 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
4387948 1004981115 RHEUMATOID ARTHRITIS
4387948 1004981118 ARTHRALGIA

Outcome of event

Event ID OUTC COD
4387948 DS
4387948 OT

Reactions reported

Event ID PT
4387948 AGGRESSION
4387948 ANXIETY
4387948 ASTHENIA
4387948 BURSITIS
4387948 CARPAL TUNNEL SYNDROME
4387948 DEPRESSION
4387948 DIFFICULTY IN WALKING
4387948 GROIN PAIN
4387948 HEART INJURY
4387948 HEART RATE IRREGULAR
4387948 HIP ARTHROPLASTY
4387948 INJURY
4387948 JOINT DISLOCATION
4387948 OSTEOARTHRITIS
4387948 PARANOIA
4387948 SACROILIITIS
4387948 STOMACH DISCOMFORT
4387948 SUICIDAL IDEATION

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID RPSR COD
4387948 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4387948 1004981114 19800101
4387948 1004981115 19990101 20010514
4387948 1004981116 19990101 20010514
4387948 1004981117 19990101 20010514
4387948 1004981118 19990101 20010514
4387948 1004981119 19990101 20010514
4387948 1004981120 19990101 20010514