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
127256301 12725630 1 I 20160525 20160831 20160908 20160908 EXP GB-PFIZER INC-2016422673 PFIZER 73.00 YR F Y 0.00000 20160908 CN 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
127256301 12725630 1 PS ATENOLOL. ATENOLOL 1 Oral 50 MG, 1X/DAY 73676 50 MG TABLET QD
127256301 12725630 2 SS ATENOLOL. ATENOLOL 1 Oral 50 MG, 1X/DAY BPQ084040 73676 50 MG TABLET QD
127256301 12725630 3 SS INDAPAMIDE. INDAPAMIDE 1 Unknown UNK Y 0
127256301 12725630 4 C ALENDRONIC ACID ALENDRONIC ACID 1 ONCE A WEEK 0 /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127256301 12725630 1 Hypertension
127256301 12725630 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127256301 12725630 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127256301 12725630 Hypersensitivity
127256301 12725630 Swollen tongue

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
127256301 12725630 2 201605 0
127256301 12725630 3 201511 20160702 0