The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
116340156 11634015 6 F 20160919 20151015 20160921 EXP US-PFIZER INC-2015343865 PFIZER 75.00 YR F Y 79.37000 KG 20160921 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
116340156 11634015 1 PS CELEBREX CELECOXIB 1 Oral 200 MG, 1X/DAY N 20998 200 MG CAPSULE, HARD QD
116340156 11634015 2 SS CELEBREX CELECOXIB 1 N 20998 CAPSULE, HARD
116340156 11634015 3 C ZYPREXA OLANZAPINE 1 UNK 0
116340156 11634015 4 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116340156 11634015 1 Arthritis
116340156 11634015 2 Arthralgia

Outcome of event

Event ID CASEID OUTC COD
116340156 11634015 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116340156 11634015 Condition aggravated
116340156 11634015 Fibromyalgia
116340156 11634015 Malaise
116340156 11634015 Pain
116340156 11634015 Peripheral swelling
116340156 11634015 Respiratory disorder

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
116340156 11634015 1 2000 0