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
127068211 12706821 1 I 20160829 20160901 20160901 EXP CA-GLAXOSMITHKLINE-CA2016GSK125593 GLAXOSMITHKLINE 64.00 YR M Y 95.00000 KG 20160901 CN CA CA

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
127068211 12706821 1 PS AVODART DUTASTERIDE 1 Oral UNK U 21319 CAPSULE QD
127068211 12706821 2 SS FLOMAX TAMSULOSIN HYDROCHLORIDE 1 Oral UNK U 0 QD
127068211 12706821 3 C NOVO-HYDRAZIDE HYDROCHLOROTHIAZIDE 1 25 MG, UNK 0 25 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127068211 12706821 1 Product used for unknown indication
127068211 12706821 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127068211 12706821 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127068211 12706821 Asthenia
127068211 12706821 Dizziness
127068211 12706821 Hepatic pain
127068211 12706821 Malaise
127068211 12706821 Orthostatic hypotension
127068211 12706821 Platelet count decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found