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
120998804 12099880 4 F 20151208 20160721 20160222 20160805 EXP DE-PFIZER INC-2016103051 PFIZER 81.00 YR F Y 0.00000 20160805 MD DE DE

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
120998804 12099880 1 PS PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Oral 80 MG, DAILY 24560 MG 20987 80 MG
120998804 12099880 2 SS PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Oral 120 MG, DAILY 24560 MG 20987 120 MG
120998804 12099880 3 C NOVAMINSULFON METAMIZOLE 1 120 GTT, QD 0 120 GTT
120998804 12099880 4 C L-THYROXIN LEVOTHYROXINE SODIUM 1 Oral 100 UG, DAILY 0 100 UG
120998804 12099880 5 C METOPROLOL SUCCINATE. METOPROLOL SUCCINATE 1 Oral 23.25 MG, QD 0 23.25 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120998804 12099880 1 Gastric ulcer
120998804 12099880 3 Osteoarthritis
120998804 12099880 4 Hypothyroidism
120998804 12099880 5 Hypertension

Outcome of event

Event ID CASEID OUTC COD
120998804 12099880 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120998804 12099880 Drug ineffective
120998804 12099880 Hyperparathyroidism
120998804 12099880 Off label use

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
120998804 12099880 1 20150205 20151209 0
120998804 12099880 2 20151210 0