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
127590671 12759067 1 I 2014 20160908 20160919 20160919 EXP BR-PFIZER INC-2016436007 PFIZER 61.00 YR F Y 0.00000 20160919 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
127590671 12759067 1 PS ATENOLOL. ATENOLOL 1 50 MG 73676 50 MG
127590671 12759067 2 SS ATACAND HCT CANDESARTAN CILEXETILHYDROCHLOROTHIAZIDE 1 Oral 16/12.5 MG EVERY DAY U 0 TABLET
127590671 12759067 3 SS CALCIUM CALCIUM 1 UNKNOWN DOSE 0
127590671 12759067 4 C NORVASC AMLODIPINE BESYLATE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127590671 12759067 2 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127590671 12759067 OT
127590671 12759067 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127590671 12759067 Blood pressure increased
127590671 12759067 Calcium intoxication
127590671 12759067 Chest pain
127590671 12759067 Fatigue
127590671 12759067 Intentional product misuse
127590671 12759067 Thyroid cancer

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

no results found

Therapies reported

no results found