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
127364731 12736473 1 I 20160823 0 20160908 20160908 DIR FDA-CTU 56.81 YR M N 57.60000 KG 20160906 N MX 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
127364731 12736473 1 PS CISPLATIN. CISPLATIN 1 0 345.3 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127364731 12736473 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127364731 12736473 Body temperature increased
127364731 12736473 Chills
127364731 12736473 Hypotension
127364731 12736473 Mucosal inflammation
127364731 12736473 Neutropenia
127364731 12736473 Oral candidiasis
127364731 12736473 Productive cough
127364731 12736473 Radiation injury
127364731 12736473 Rhinorrhoea
127364731 12736473 Skin erosion

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
127364731 12736473 1 20160810 0