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
124564653 12456465 3 F 201501 20160707 20160610 20160711 PER US-PFIZER INC-2016278103 PFIZER 57.00 YR F Y 84.00000 KG 20160711 CN 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
124564653 12456465 1 PS AROMASIN EXEMESTANE 1 Oral 25 MG, 1X/DAY N Z995L 20753 25 MG COATED TABLET QD
124564653 12456465 2 SS AROMASIN EXEMESTANE 1 N 20753 COATED TABLET
124564653 12456465 3 SS LETROZOLE. LETROZOLE 1 Oral 2.5 MG, 1X/DAY U 0 2.5 MG TABLET QD
124564653 12456465 4 SS LETROZOLE. LETROZOLE 1 UNK U 0 TABLET
124564653 12456465 5 SS LETROZOLE. LETROZOLE 1 UNK U 0 TABLET
124564653 12456465 6 C SYNTHROID LEVOTHYROXINE SODIUM 1 112 UG, 1X/DAY 0 112 UG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124564653 12456465 1 Neoplasm malignant
124564653 12456465 2 Blood oestrogen decreased
124564653 12456465 3 Neoplasm malignant
124564653 12456465 4 Blood oestrogen decreased
124564653 12456465 6 Hypothyroidism

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124564653 12456465 Arthralgia
124564653 12456465 Fatigue
124564653 12456465 Feeling abnormal
124564653 12456465 Hepatic enzyme increased
124564653 12456465 Musculoskeletal stiffness

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
124564653 12456465 1 20160105 201603 0
124564653 12456465 3 2016 0
124564653 12456465 4 2014 20160104 0
124564653 12456465 5 201603 0
124564653 12456465 6 20100609 0