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
125656701 12565670 1 I 2016 20160707 20160718 20160718 EXP US-PFIZER INC-2016337418 PFIZER 83.00 YR M Y 90.26000 KG 20160718 CN 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
125656701 12565670 1 PS LIPITOR ATORVASTATIN CALCIUM 1 UNK Y 20702 FILM-COATED TABLET
125656701 12565670 2 C AVODART DUTASTERIDE 1 10 MG, UNK 0 10 MG
125656701 12565670 3 C ASPIRIN. ASPIRIN 1 81 MG, UNK 0 81 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125656701 12565670 1 Blood cholesterol
125656701 12565670 2 Dysuria
125656701 12565670 3 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
125656701 12565670 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125656701 12565670 Abasia
125656701 12565670 Abdominal pain
125656701 12565670 Arthralgia
125656701 12565670 Back pain
125656701 12565670 Cough
125656701 12565670 Dysphagia
125656701 12565670 Inflammation
125656701 12565670 Joint swelling
125656701 12565670 Movement disorder
125656701 12565670 Peripheral swelling

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
125656701 12565670 1 2016 0