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
106410276 10641027 6 F 200902 20160627 20141209 20160701 EXP US-009507513-1412USA003666 MERCK 0.00 M Y 98.41000 KG 20160701 MD 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
106410276 10641027 1 PS PROPECIA FINASTERIDE 1 Oral 1 MG, 1 TAB, QD N 20788 1 MG FILM-COATED TABLET QD
106410276 10641027 2 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106410276 10641027 1 Alopecia
106410276 10641027 2 Gastrooesophageal reflux disease

Outcome of event

Event ID CASEID OUTC COD
106410276 10641027 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106410276 10641027 Asthenia
106410276 10641027 Back pain
106410276 10641027 Blood testosterone abnormal
106410276 10641027 Eczema
106410276 10641027 Elbow operation
106410276 10641027 Erectile dysfunction
106410276 10641027 Fatigue
106410276 10641027 Flushing
106410276 10641027 Growth hormone-producing pituitary tumour
106410276 10641027 Hypothalamo-pituitary disorder
106410276 10641027 Libido decreased
106410276 10641027 Rosacea
106410276 10641027 Secondary hypogonadism
106410276 10641027 Sexual dysfunction
106410276 10641027 Skin disorder

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
106410276 10641027 1 20040824 201008 0
106410276 10641027 2 199502 0