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
126096351 12609635 1 I 20150630 20160801 20160801 PER US-DRREDDYS-USA/USA/15/0049098 DR REDDYS 0.00 M Y 88.45000 KG 20160801 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
126096351 12609635 1 PS OMEPRAZOLE MAGNESIUM DELAYED RELEASE OTC OMEPRAZOLE MAGNESIUM 1 Oral 79C408286A 78878 20.6 MG CAPSULE QD
126096351 12609635 2 SS OMEPRAZOLE MAGNESIUM DELAYED RELEASE OTC OMEPRAZOLE MAGNESIUM 1 Oral 79C408286A 78878 20.6 MG CAPSULE BID
126096351 12609635 3 C ASPIRIN. ASPIRIN 1 Unknown 0
126096351 12609635 4 C TYLENOL ACETAMINOPHEN 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126096351 12609635 1 Gastrooesophageal reflux disease
126096351 12609635 3 Product used for unknown indication
126096351 12609635 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126096351 12609635 Drug ineffective
126096351 12609635 Extra dose administered
126096351 12609635 Product quality issue

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
126096351 12609635 1 201506 0
126096351 12609635 2 201506 0