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
125598631 12559863 1 I 20160628 20160706 20160715 20160715 EXP GB-PFIZER INC-2016340152 PFIZER 69.00 YR M Y 0.00000 20160715 MD 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
125598631 12559863 1 PS RAMIPRIL. RAMIPRIL 1 Unknown UNK U 19901
125598631 12559863 2 C FINASTERIDE. FINASTERIDE 1 UNK 0
125598631 12559863 3 C SOLIFENACIN SOLIFENACIN 1 UNK 0
125598631 12559863 4 C TAMSULOSIN HYDROCHLORIDE. TAMSULOSIN HYDROCHLORIDE 1 UNK 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125598631 12559863 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125598631 12559863 Abdominal pain
125598631 12559863 Balance disorder
125598631 12559863 Chest pain
125598631 12559863 Confusional state
125598631 12559863 Muscle spasms
125598631 12559863 Myalgia

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
125598631 12559863 1 20160114 0
125598631 12559863 2 20160114 0
125598631 12559863 3 20160114 0
125598631 12559863 4 20160114 0