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
127409491 12740949 1 I 20160902 20160906 20160914 20160914 EXP US-ASTRAZENECA-2016SE95787 ASTRAZENECA 19409.00 DY F Y 67.00000 KG 20160914 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
127409491 12740949 1 PS ZOLADEX GOSERELIN ACETATE 1 Subcutaneous 198 MG 20578 3.6 MG IMPLANT /month
127409491 12740949 2 C MORPHINE INJECTION MORPHINE 1 INTERMITTENT, TAKEN EVERY 6 HOURS AS REQUIRED 0 INJECTION
127409491 12740949 3 C ATIVAN, LORAZEPAM 2 INTERMITTENT 0
127409491 12740949 4 C HALDOL HALOPERIDOL 1 Intramuscular INTERMITTENT 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127409491 12740949 1 Breast cancer female
127409491 12740949 2 Pain
127409491 12740949 3 Anxiety
127409491 12740949 4 Agitation

Outcome of event

Event ID CASEID OUTC COD
127409491 12740949 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127409491 12740949 Death

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
127409491 12740949 1 201111 20160622 0
127409491 12740949 2 201607 0