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
126429641 12642964 1 I 20160729 20160809 20160811 20160811 EXP GB-ASTRAZENECA-2016SE85961 ASTRAZENECA 69.00 YR M Y 83.00000 KG 20160811 PH GB GB

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
126429641 12642964 1 PS OMEPRAZOLE. OMEPRAZOLE 1 Oral U U 19810 20 MG QD
126429641 12642964 2 C ATORVASTATIN ATORVASTATIN 1 0
126429641 12642964 3 C BISOPROLOL BISOPROLOL 1 0
126429641 12642964 4 C CALCICHEW D3 CALCIUMCHOLECALCIFEROL 1 0
126429641 12642964 5 C GLICLAZIDE GLICLAZIDE 1 0
126429641 12642964 6 C LEVOTHYROXINE. LEVOTHYROXINE 1 0
126429641 12642964 7 C SITAGLIPTIN SITAGLIPTIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126429641 12642964 1 Gastrooesophageal reflux disease

Outcome of event

Event ID CASEID OUTC COD
126429641 12642964 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126429641 12642964 Hypomagnesaemia
126429641 12642964 Seizure

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

no results found

Therapies reported

no results found