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
92746901 9274690 1 I 20130425 0 20130430 20130430 DIR 59.00 YR F N 116.50000 KG 20130428 RN 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
92746901 9274690 1 PS EVEROLIMUS 1 ORAL 5MG ORAL DAILY D D 0 5 MG QD
92746901 9274690 3 C IMODIUM 1 0
92746901 9274690 5 C PROMETHAZINE 1 0
92746901 9274690 7 C ONDANSETRON HCL 1 0
92746901 9274690 9 C HYDROCODONE-ACETAMINOPHEN 1 0
92746901 9274690 10 C DIOVAN 1 0
92746901 9274690 11 C AMLODIPINE 1 0
92746901 9274690 12 C MAGNESIUM CHLORIDE 1 0
92746901 9274690 13 C KLOR-CON 1 0
92746901 9274690 15 C HYDROXYZINE 1 0
92746901 9274690 17 C DEXAMETHASONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
92746901 9274690 1 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
92746901 9274690 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
92746901 9274690 Diarrhoea

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID CASEID RPSR COD
92746901 9274690 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
92746901 9274690 1 20130122 20130419 0