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
125234001 12523400 1 I 20160624 20160703 20160703 PER US-ASTRAZENECA-2016SE70274 ASTRAZENECA 0.00 F Y 55.30000 KG 20160703 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
125234001 12523400 1 SS LISINOPRIL HCTZ HYDROCHLOROTHIAZIDELISINOPRIL 1 Oral 10/12.5 MG.,1 HALF TABLET TAKEN DAILY U U 0 TABLET
125234001 12523400 2 PS TOPROL XL METOPROLOL SUCCINATE 1 Oral 50, MG DAILY U 19962 MODIFIED-RELEASE TABLET
125234001 12523400 3 SS METOPROLOL. METOPROLOL 1 Oral U 0
125234001 12523400 4 C LORAZEPAM. LORAZEPAM 1 Oral 0.5MG INTERMITTENT U 0 .5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125234001 12523400 1 Blood pressure abnormal

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125234001 12523400 Arrhythmia
125234001 12523400 Atrial fibrillation
125234001 12523400 Blood pressure increased
125234001 12523400 Drug ineffective
125234001 12523400 Heart rate increased

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
125234001 12523400 1 2014 0
125234001 12523400 2 201601 0
125234001 12523400 3 2014 0