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
122110934 12211093 4 F 20160720 20160325 20160726 EXP GB-PFIZER INC-2016168654 PFIZER 0.00 F Y 0.00000 20160726 OT GB GB

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
122110934 12211093 1 PS EXEMESTANE. EXEMESTANE 1 25 MG, 1X/DAY U 20753 25 MG COATED TABLET QD
122110934 12211093 2 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous 600 MG, UNK U 0 600 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
122110934 12211093 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122110934 12211093 Abdominal pain upper
122110934 12211093 Constipation
122110934 12211093 Decreased appetite
122110934 12211093 Depressed mood
122110934 12211093 Dysgeusia
122110934 12211093 Fatigue
122110934 12211093 Food intolerance
122110934 12211093 Hair disorder
122110934 12211093 Joint swelling
122110934 12211093 Malaise
122110934 12211093 Nausea
122110934 12211093 Oropharyngeal pain
122110934 12211093 Pain
122110934 12211093 Paraesthesia
122110934 12211093 Pollakiuria
122110934 12211093 Scab
122110934 12211093 Somnolence
122110934 12211093 White blood cells urine

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
122110934 12211093 1 20160624 0