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
125258021 12525802 1 I 20160523 20160705 20160705 PER US-ASTRAZENECA-2016SE56154 ASTRAZENECA 0.00 F Y 0.00000 20160705 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
125258021 12525802 1 PS IRESSA GEFITINIB 1 Oral U 206995 250 MG TABLET QD
125258021 12525802 2 SS IRESSA GEFITINIB 1 Oral U 206995 250 MG TABLET QD
125258021 12525802 3 C AMLODIPINE BESYLATE. AMLODIPINE BESYLATE 1 0
125258021 12525802 4 C CALCIUM WITH VITAMIN D CALCIUMVITAMIN D 1 0
125258021 12525802 5 C LEVOTHYROXINE. LEVOTHYROXINE 1 0
125258021 12525802 6 C ZANTAC RANITIDINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125258021 12525802 1 Non-small cell lung cancer
125258021 12525802 2 Non-small cell lung cancer

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125258021 12525802 Chest discomfort
125258021 12525802 Dyspnoea
125258021 12525802 Feeling abnormal
125258021 12525802 Rash macular

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
125258021 12525802 1 20160505 20160522 0
125258021 12525802 2 20160523 0