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
5040495 6045522 F 5040495-6 20060301 20060502 20060630 EXP US-ROCHE-446548 ROCHE 72 YR F Y 20060630 CN 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
5040495 1007431408 PS BONIVA 1 ORAL 21455
5040495 1007431409 C VITAMINS NOS 2 ORAL
5040495 1007431410 C ZYRTEC 1 ORAL
5040495 1007431411 C SINGULAIR 1 ORAL
5040495 1007431412 C PRILOSEC 1
5040495 1007431413 C LIPITOR 1
5040495 1007431414 C CLARINEX 1
5040495 1007431415 C ASPIRIN 1
5040495 1007431416 C CELEBREX 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
5040495 1007431408 OSTEOPOROSIS
5040495 1007431410 ASTHMA
5040495 1007431411 ASTHMA
5040495 1007431416 RHEUMATOID ARTHRITIS

Outcome of event

Event ID OUTC COD
5040495 OT

Reactions reported

Event ID PT
5040495 ARTHRALGIA
5040495 CARPAL TUNNEL SYNDROME

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
5040495 1007431408 20060301 20060401 32 DAY
5040495 1007431416 19960615