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
125785522 12578552 2 F 20160209 20160715 20160721 20160722 EXP US-ASTRAZENECA-2016SE16894 ASTRAZENECA 16107.00 DY M Y 0.00000 20160722 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
125785522 12578552 1 PS TAGRISSO OSIMERTINIB 1 Oral 960 MG FN0072 208065 80 MG TABLET QD
125785522 12578552 2 SS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral U 0
125785522 12578552 3 C ANDROGEL TESTOSTERONE 1 0 TRANSDERMAL PATCH
125785522 12578552 4 C OXYCODONE OXYCODONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125785522 12578552 1 Lung carcinoma cell type unspecified stage I
125785522 12578552 4 Pain

Outcome of event

Event ID CASEID OUTC COD
125785522 12578552 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125785522 12578552 Abdominal pain upper
125785522 12578552 Arthralgia
125785522 12578552 Fatigue
125785522 12578552 Pulmonary embolism
125785522 12578552 Rash

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
125785522 12578552 1 20160129 0