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
127826841 12782684 1 I 20160906 0 20160923 20160923 DIR FDA-CTU 69.52 YR F N 69.50000 KG 20160922 N 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
127826841 12782684 1 PS PACLITAXEL. PACLITAXEL 1 0 970 MG
127826841 12782684 2 SS DOXORUBICIN HYDROCHLORIDE. DOXORUBICIN HYDROCHLORIDE 1 DOXORUBICIN HYDROCHLORIDE - DOSE REDUCED CYCLE 4 0 97 MG
127826841 12782684 3 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 CYCLOPHOSPHAMIDE - DOSE REDUCED CYCLE 4 0 970 MG
127826841 12782684 5 C AZITHROMYCIN ANHYDROUS. AZITHROMYCIN ANHYDROUS 1 0
127826841 12782684 7 C CIPROFLOXIN CIPROFLOXACIN 1 0
127826841 12782684 9 C LEVAQUIN LEVOFLOXACIN 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127826841 12782684 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127826841 12782684 Anaemia
127826841 12782684 Ascites
127826841 12782684 Clostridium difficile infection
127826841 12782684 Hypokalaemia
127826841 12782684 Hypotension
127826841 12782684 Leukocytosis
127826841 12782684 Pleural effusion
127826841 12782684 Pneumonia streptococcal
127826841 12782684 Sepsis
127826841 12782684 Seroma

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
127826841 12782684 1 20160825 0
127826841 12782684 2 20160712 0
127826841 12782684 3 20160712 0