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
125402431 12540243 1 I 20160615 20160627 20160708 20160708 EXP NL-LRB-221165 NL-PFIZER INC-2016334227 PFIZER 67.00 YR F Y 0.00000 20160708 PH NL NL

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
125402431 12540243 1 PS PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Oral 40 MG, BID 160 MG Y 20987 40 MG TABLET BID
125402431 12540243 2 C EZETROL EZETIMIBE 1 Oral 10 MG, QD 0 10 MG TABLET QD
125402431 12540243 3 C ATORVASTATINE OMHULD 2 Oral 20 MG, QD 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125402431 12540243 1 Gastrooesophageal reflux disease

Outcome of event

Event ID CASEID OUTC COD
125402431 12540243 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125402431 12540243 Headache
125402431 12540243 Malaise
125402431 12540243 Neck pain
125402431 12540243 Pyrexia
125402431 12540243 Renal pain
125402431 12540243 Urinary retention

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
125402431 12540243 1 20160614 20160617 0
125402431 12540243 2 20160614 0
125402431 12540243 3 20020403 0