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
124842212 12484221 2 F 201605 20160617 20160621 20160811 PER US-ASTRAZENECA-2016SE56025 ASTRAZENECA 27212.00 DY M Y 72.10000 KG 20160811 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
124842212 12484221 1 SS TENORETIC ATENOLOLCHLORTHALIDONE 1 Oral DAILY 0 TABLET
124842212 12484221 2 SS ATENOLOL. ATENOLOL 1 U U 0 50 MG QD
124842212 12484221 3 SS LISINOPRIL. LISINOPRIL 1 Oral U U 0 10 MG TABLET QD
124842212 12484221 4 PS OMEPRAZOLE. OMEPRAZOLE 1 Oral 20.0MG AS REQUIRED 19810 20 MG
124842212 12484221 5 SS BRILINTA TICAGRELOR 1 Oral HC0034 0 90 MG TABLET BID
124842212 12484221 6 SS BRILINTA TICAGRELOR 1 Oral HC0034 0 90 MG TABLET BID
124842212 12484221 7 C ASPIRIN. ASPIRIN 1 Oral 0 85 MG QD
124842212 12484221 8 C ASPIRIN. ASPIRIN 1 Oral 0 81 MG QD
124842212 12484221 9 C POTASSIUM POTASSIUM 1 Oral 0 20 MEQ QD
124842212 12484221 10 C LIPITOR ATORVASTATIN CALCIUM 1 Oral 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124842212 12484221 1 Hypertension
124842212 12484221 2 Hypertension
124842212 12484221 3 Hypertension
124842212 12484221 4 Gastrooesophageal reflux disease
124842212 12484221 5 Stent placement
124842212 12484221 6 Acute coronary syndrome
124842212 12484221 7 Cardiac disorder
124842212 12484221 8 Cardiac disorder
124842212 12484221 9 Muscle spasms
124842212 12484221 10 Blood cholesterol abnormal

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124842212 12484221 Abdominal pain upper
124842212 12484221 Drug dose omission
124842212 12484221 Gallbladder disorder
124842212 12484221 Rash
124842212 12484221 Urticaria
124842212 12484221 Weight 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
124842212 12484221 3 20160608 0
124842212 12484221 5 20160421 0
124842212 12484221 6 20160421 0