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
127313671 12731367 1 I 20160831 20160912 20160912 PER US-ASTRAZENECA-2016SE95850 ASTRAZENECA 0.00 F Y 0.00000 20160912 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
127313671 12731367 1 PS NEXIUM 24HR ESOMEPRAZOLE MAGNESIUM 1 Oral U 204655 1 DF CAPSULE QD
127313671 12731367 2 SS CALTRATE 600 + D PLUS MINERAL CALCIUMCHOLECALCIFEROLCOPPERMAGNESIUMMANGANESEINC 1 Unknown 1.0DF UNKNOWN L99038 0 1 DF TABLET
127313671 12731367 3 SS CENTRUM SILVER WOMEN'S 50+ MINERALSVITAMINS 1 Unknown UNK M45061 0 TABLET
127313671 12731367 4 SS VITAMIN C ASCORBIC ACID 1 Unknown U 0
127313671 12731367 5 C OTHER MEDICATION UNSPECIFIED INGREDIENT 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127313671 12731367 1 Gastrooesophageal reflux disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127313671 12731367 Abdominal distension
127313671 12731367 Abdominal pain upper
127313671 12731367 Drug intolerance
127313671 12731367 Product use issue

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

no results found

Therapies reported

no results found