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
121179092 12117909 2 F 20151208 20160719 20160226 20160802 EXP DE-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-112260 RANBAXY 81.00 YR F Y 0.00000 20160802 OT 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
121179092 12117909 1 PS Pantoprazole PANTOPRAZOLE SODIUM 1 Oral 40 MG, BID 24560 MG 200794 40 MG Q12H
121179092 12117909 2 SS Pantoprazole PANTOPRAZOLE SODIUM 1 Oral 60 MG, BID 200794 60 MG Q12H
121179092 12117909 3 C METOPROLOL SUCCINATE. METOPROLOL SUCCINATE 1 Oral 23.25 MG, QD U U 0 23.25 MG
121179092 12117909 4 C L-thyroxin LEVOTHYROXINE SODIUM 1 Oral 100 ?G, QD U U 0 100 UG
121179092 12117909 5 C Novaminsulfon METAMIZOLE 1 Oral U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121179092 12117909 1 Gastric ulcer
121179092 12117909 2 Gastric ulcer
121179092 12117909 3 Hypertension
121179092 12117909 4 Hypothyroidism
121179092 12117909 5 Osteoarthritis

Outcome of event

Event ID CASEID OUTC COD
121179092 12117909 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121179092 12117909 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
121179092 12117909 1 20150205 20151209 0
121179092 12117909 2 20151210 0