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
124929762 12492976 2 F 201601 20160609 20160623 20160721 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-37425BP BOEHRINGER INGELHEIM 83.70 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
124929762 12492976 1 PS ZANTAC RANITIDINE HYDROCHLORIDE 1 Oral DAILY DOSE- 150 MG TWICE PRN 559390 21698 150 MG TABLET
124929762 12492976 2 SS ZANTAC RANITIDINE HYDROCHLORIDE 1 559390 21698
124929762 12492976 3 SS ZANTAC RANITIDINE HYDROCHLORIDE 1 559390 21698
124929762 12492976 4 C LISINOPRIL. LISINOPRIL 1 Oral 2.5 MG 0 2.5 MG TABLET QD
124929762 12492976 5 C LORAZEPAM. LORAZEPAM 1 Oral 0 .05 MG TABLET
124929762 12492976 6 C Centrum Silver MINERALSVITAMINS 1 Oral 0 TABLET QD
124929762 12492976 7 C Citrical CALCIUM CITRATE 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124929762 12492976 1 Pain
124929762 12492976 2 Gastrooesophageal reflux disease
124929762 12492976 3 Abdominal distension
124929762 12492976 4 Hypertension
124929762 12492976 5 Initial insomnia
124929762 12492976 6 Supplementation therapy
124929762 12492976 7 Osteoporosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124929762 12492976 Incorrect drug administration duration
124929762 12492976 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
124929762 12492976 1 20160129 0
124929762 12492976 4 2014 0
124929762 12492976 5 2011 0