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
122434622 12243462 2 F 20150927 20160914 20160406 20160919 EXP GB-PFIZER INC-2016190193 PFIZER 71.00 YR F Y 0.00000 20160919 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
122434622 12243462 1 PS TOVIAZ FESOTERODINE FUMARATE 1 8 MG, 1X/DAY 22030 8 MG PROLONGED-RELEASE TABLET QD
122434622 12243462 2 I BETMIGA MIRABEGRON 1 50 MG, 1X/DAY 350 MG Y 0 50 MG QD
122434622 12243462 3 C ADCAL D3 CALCIUM CARBONATECHOLECALCIFEROL 1 Oral UNK UNK, UNKNOWN FREQ. 0
122434622 12243462 4 C ASPIRIN (E.C.) ASPIRIN 1 Unknown UNK UNK, UNKNOWN FREQ. 0
122434622 12243462 5 C LANSOPRAZOLE. LANSOPRAZOLE 1 Unknown UNK UNK, UNKNOWN FREQ. 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122434622 12243462 1 Hypertonic bladder
122434622 12243462 3 Osteoporosis
122434622 12243462 4 Angina pectoris
122434622 12243462 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
122434622 12243462 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122434622 12243462 Cystitis
122434622 12243462 Drug interaction
122434622 12243462 Haematuria
122434622 12243462 Shock

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
122434622 12243462 2 20150920 0