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
101121842 10112184 2 F 20140419 20140923 20140425 20140930 EXP PHHO2014FR005987 NOVARTIS 66.40 YR F Y 0.00000 20140930 N OT FR FR

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
101121842 10112184 1 PS CGS 20267 LETROZOLE 1 2.5 MG, QD D 20726 2.5 MG TABLET QD
101121842 10112184 2 SS EVEROLIMUS EVEROLIMUS 1 10 MG, QD 580 MG D 0 10 MG TABLET QD
101121842 10112184 3 C ALTEIS OLMESARTAN MEDOXOMIL 1 ORAL 26 MG, QD D 0 26 MG QD
101121842 10112184 4 C CORTICOSTEROID NOS CORTICOSTEROID NOS 1 D 0
101121842 10112184 5 C DIFFU K POTASSIUM CHLORIDE 1 D 0
101121842 10112184 6 C CRESTOR ROSUVASTATIN CALCIUM 1 D 0
101121842 10112184 7 C SOLUPRED PREDNISOLONE 1 D 0
101121842 10112184 8 C LOVENOX ENOXAPARIN SODIUM 1 ORAL 0.4 ML, QD D 0 .4 ML QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101121842 10112184 1 Breast cancer metastatic
101121842 10112184 2 Breast cancer metastatic
101121842 10112184 3 Hypertension
101121842 10112184 7 Cough
101121842 10112184 8 Pulmonary embolism

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
101121842 10112184 Blood pressure decreased

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
101121842 10112184 1 20140204 0
101121842 10112184 2 20140204 20140402 0