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
126087121 12608712 1 I 20160722 20160729 20160729 EXP US-ASTRAZENECA-2016SE80614 ASTRAZENECA 0.00 F Y 0.00000 20160729 MD 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
126087121 12608712 1 PS ANASTROZOLE. ANASTROZOLE 1 Oral U U 20541 1 MG TABLET QD
126087121 12608712 2 SS AROMASIN EXEMESTANE 1 Oral U 0 25 MG TABLET QD
126087121 12608712 3 SS FELDENE PIROXICAM 1 Oral U 0 10 MG CAPSULE QD
126087121 12608712 4 SS LIPITOR ATORVASTATIN CALCIUM 1 Oral U 0 10 MG TABLET QD
126087121 12608712 5 C ACETAMINOPHEN-CODEINE ACETAMINOPHENCODEINE PHOSPHATE 1 Oral 300-30 MG 1 DF, EVERY 4 HOURS AS NEEDED 0 TABLET
126087121 12608712 6 C ENALAPRIL- HYDROCHLOROTHIAZIDE 2 Oral 10-25MG 1 DF, DAILY 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126087121 12608712 1 Breast cancer female

Outcome of event

Event ID CASEID OUTC COD
126087121 12608712 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126087121 12608712 Arthralgia
126087121 12608712 Axillary pain
126087121 12608712 Breast pain
126087121 12608712 Hypertension
126087121 12608712 Osteoarthritis

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

no results found

Therapies reported

no results found