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
124062632 12406263 2 F 201604 20160511 20160526 20160721 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-30310BP BOEHRINGER INGELHEIM 80.50 YR F Y 0.00000 20160721 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
124062632 12406263 1 PS ZANTAC RANITIDINE HYDROCHLORIDE 1 Oral 150 MG 654709 21698 150 MG TABLET QD
124062632 12406263 2 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral 1 ANZ 0 TABLET QD
124062632 12406263 3 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral 2 ANZ 0 TABLET BID
124062632 12406263 4 C GAVISCON ALUMINUM HYDROXIDEMAGNESIUM CARBONATE 1 Oral 1 ANZ 0 ORAL SUSPENSION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124062632 12406263 1 Gastrooesophageal reflux disease
124062632 12406263 2 Gastrooesophageal reflux disease
124062632 12406263 4 Gastrooesophageal reflux disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124062632 12406263 Dyspnoea
124062632 12406263 Incorrect drug administration duration
124062632 12406263 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
124062632 12406263 1 201604 0
124062632 12406263 2 201604 20160503 0
124062632 12406263 3 20160504 0