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
127050351 12705035 1 I 20160810 20160829 20160831 20160831 EXP US-ALLERGAN-1667192US ALLERGAN 36.00 YR M Y 73.48000 KG 20160831 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
127050351 12705035 1 PS NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 5/325 MG, EVERY 6 HOURS PRN N U 40148 TABLET
127050351 12705035 2 SS NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 N U 40148 TABLET
127050351 12705035 3 SS SUTENT SUNITINIB MALATE 1 Oral 50 MG, QD FOR 28 DAYS 0 50 MG QD
127050351 12705035 4 SS SUTENT SUNITINIB MALATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127050351 12705035 1 Pain
127050351 12705035 2 Chest pain
127050351 12705035 3 Sarcoma
127050351 12705035 4 Gastrointestinal stromal tumour

Outcome of event

Event ID CASEID OUTC COD
127050351 12705035 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127050351 12705035 Drug ineffective
127050351 12705035 Hepatic infection
127050351 12705035 Pain
127050351 12705035 Pleural effusion

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
127050351 12705035 1 20160808 20160808 0
127050351 12705035 3 201604 0