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
126999931 12699993 1 I 20100404 20100620 20160830 20160830 EXP US-PFIZER INC-2010076688 PFIZER 59.00 YR F Y 67.00000 KG 20160830 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
126999931 12699993 1 PS IBUPROFEN. IBUPROFEN 1 Oral UNK Y 18989 TABLET
126999931 12699993 2 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 20 MG, DAILY 0 20 MG
126999931 12699993 3 C FLEXERIL CYCLOBENZAPRINE HYDROCHLORIDE 1 Oral 10 MG, ONCE IN THE EVENING AS NEEDED 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126999931 12699993 1 Osteoarthritis
126999931 12699993 2 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126999931 12699993 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126999931 12699993 Chest pain

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
126999931 12699993 1 20091216 20100404 0
126999931 12699993 2 20091216 20100404 0
126999931 12699993 3 200906 0