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
121231072 12123107 2 F 20151208 20160719 20160227 20160727 EXP DE-AUROBINDO-AUR-APL-2016-01845 AUROBINDO 81.00 YR F Y 0.00000 20160727 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
121231072 12123107 1 PS Pantoprazole PANTOPRAZOLE SODIUM 1 Oral 80 MG, DAILY 202038 80 MG
121231072 12123107 2 SS Pantoprazole PANTOPRAZOLE SODIUM 1 Oral 120 MG, DAILY 202038 120 MG
121231072 12123107 3 C METOPROLOL SUCCINATE. METOPROLOL SUCCINATE 1 Oral 23.25 MG, DAILY U U 0 23.25 MG
121231072 12123107 4 C L-THYROXIN LEVOTHYROXINE SODIUM 1 Oral 100 ?G, DAILY U U 0 100 UG
121231072 12123107 5 C NOVAMINSULFON METAMIZOLE 1 Oral 4X30 U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121231072 12123107 1 Gastric ulcer
121231072 12123107 3 Hypertension
121231072 12123107 4 Hypothyroidism
121231072 12123107 5 Osteoarthritis

Outcome of event

Event ID CASEID OUTC COD
121231072 12123107 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121231072 12123107 Hyperparathyroidism

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
121231072 12123107 1 20150205 20151209 0
121231072 12123107 2 20151210 0