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
127497251 12749725 1 I 2014 20160908 20160915 20160915 EXP BR-ASTRAZENECA-2016SE97205 ASTRAZENECA 61.00 YR F Y 0.00000 20160915 CN BR BR

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
127497251 12749725 1 SS ATENOLOL. ATENOLOL 1 Unknown 50 MG 0
127497251 12749725 2 PS ATACAND HCT CANDESARTAN CILEXETILHYDROCHLOROTHIAZIDE 1 Oral 16/12.5 MG EVERY DAY U U 21093 TABLET
127497251 12749725 3 SS CALCIUM CALCIUM 1 Unknown 0
127497251 12749725 4 C NORVASC AMLODIPINE BESYLATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127497251 12749725 2 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127497251 12749725 OT
127497251 12749725 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127497251 12749725 Blood pressure increased
127497251 12749725 Calcium intoxication
127497251 12749725 Chest pain
127497251 12749725 Fatigue
127497251 12749725 Intentional product misuse
127497251 12749725 Thyroid cancer

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

no results found

Therapies reported

no results found