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
127070641 12707064 1 I 20130725 20130821 20160901 20160901 EXP US-PFIZER INC-2013241581 PFIZER 48.00 YR M Y 111.80000 KG 20160901 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
127070641 12707064 1 PS IBUPROFEN. IBUPROFEN 1 Oral UNK Y 18989 TABLET
127070641 12707064 2 SS IBUPROFEN. IBUPROFEN 1 Y 18989 TABLET
127070641 12707064 3 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral 1 TAB, QD 0 1 DF TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127070641 12707064 1 Osteoarthritis
127070641 12707064 2 Rheumatoid arthritis
127070641 12707064 3 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
127070641 12707064 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127070641 12707064 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
127070641 12707064 1 20120821 20130819 0
127070641 12707064 3 2000 0