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
126063521 12606352 1 I 20160112 20160729 20160729 PER US-DRREDDYS-USA/USA/16/0055857 DR REDDYS 0.00 F Y 0.00000 20160729 CN 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
126063521 12606352 1 PS OMEPRAZOLE MAGNESIUM DELAYED RELEASE OTC OMEPRAZOLE MAGNESIUM 1 Oral U U UNKNOWN 78878 20.6 MG CAPSULES QD
126063521 12606352 2 C GABAPENTIN. GABAPENTIN 1 Unknown 0
126063521 12606352 3 C DICYCLOMINE DICYCLOMINE HYDROCHLORIDE 1 Unknown 0
126063521 12606352 4 C Align probiotic 2 Unknown 0
126063521 12606352 5 C METOPROLOL. METOPROLOL 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126063521 12606352 1 Dyspepsia
126063521 12606352 2 Product used for unknown indication
126063521 12606352 3 Product used for unknown indication
126063521 12606352 4 Product used for unknown indication
126063521 12606352 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126063521 12606352 Dyspepsia
126063521 12606352 Product quality issue

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found