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
125253072 12525307 2 F 20160329 20160627 20160704 20160830 EXP JP-ASTRAZENECA-2016SE71426 ASTRAZENECA 72.00 YR F Y 52.00000 KG 20160831 PH JP JP

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
125253072 12525307 1 PS IRESSA GEFITINIB 1 Oral 31500 MG N U 206995 250 MG TABLET QD
125253072 12525307 2 C ETIZOLAM ETIZOLAM 1 Unknown 0 .5 MG QD
125253072 12525307 3 C FAMOTIDINE. FAMOTIDINE 1 Unknown 0 20 MG BID
125253072 12525307 4 C SENNOSIDE SENNOSIDES 1 Unknown 0 12 MG QD
125253072 12525307 5 C MAGMITT MAGNESIUM OXIDE 1 Unknown 0 330 MG TID
125253072 12525307 6 C MS-TWICELON 2 Oral 0 10 MG CAPSULE BID
125253072 12525307 7 C OPSO MORPHINE HYDROCHLORIDE 1 Unknown NUMBER OF SEPARATE DOSAGES UNKNOWN 0 5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125253072 12525307 1 Lung adenocarcinoma

Outcome of event

Event ID CASEID OUTC COD
125253072 12525307 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125253072 12525307 Decreased appetite
125253072 12525307 Eczema
125253072 12525307 Excessive granulation tissue

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
125253072 12525307 1 20160120 20160524 0