The Safety Rates Drug Report

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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
125056912 12505691 2 F 20160711 20160628 20160804 PER US-PFIZER INC-2016242041 PFIZER 83.00 YR F Y 0.00000 20160804 MD 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
125056912 12505691 1 PS CELEBREX CELECOXIB 1 Oral 100 MG, 2X/DAY 20998 100 MG CAPSULE, HARD BID
125056912 12505691 2 SS CELEBREX CELECOXIB 1 20998 CAPSULE, HARD
125056912 12505691 3 SS CELEBREX CELECOXIB 1 20998 CAPSULE, HARD
125056912 12505691 4 SS CELEBREX CELECOXIB 1 20998 CAPSULE, HARD
125056912 12505691 5 SS DULOXETINE. DULOXETINE 1 100 MG, UNK 0 100 MG
125056912 12505691 6 C DIAZEPAM. DIAZEPAM 1 UNK 0
125056912 12505691 7 C LISINOPRIL. LISINOPRIL 1 UNK 0
125056912 12505691 8 C HCTZ HYDROCHLOROTHIAZIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125056912 12505691 1 Osteoarthritis
125056912 12505691 2 Polymyalgia rheumatica
125056912 12505691 3 Essential hypertension
125056912 12505691 4 Fibromyalgia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125056912 12505691 Abdominal pain
125056912 12505691 Headache
125056912 12505691 Vision blurred

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
125056912 12505691 1 20110316 0