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
125943882 12594388 2 F 201510 20160831 20160726 20160909 PER US-009507513-1606USA012981 MERCK 80.57 YR F Y 0.00000 20160909 OT 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
125943882 12594388 1 PS PROVENTIL ALBUTEROL 1 3 X DAY U 20503 INHALATION POWDER TID
125943882 12594388 2 SS METOPROLOL. METOPROLOL 1 100 MG, QD 0 100 MG QD
125943882 12594388 3 SS SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 1 X DAY 0 QD
125943882 12594388 4 SS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 250 MG, BID 0 250 MG BID
125943882 12594388 5 C OMEPRAZOLE. OMEPRAZOLE 1 Oral 20 MG, QD U 0 20 MG CAPSULE QD
125943882 12594388 6 C hydrochlorothiazide (+) triamterene HYDROCHLOROTHIAZIDETRIAMTERENE 1 37.5/25 MG, QD U 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125943882 12594388 1 Chronic obstructive pulmonary disease
125943882 12594388 2 Blood pressure abnormal
125943882 12594388 3 Chronic obstructive pulmonary disease
125943882 12594388 4 Chronic obstructive pulmonary disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125943882 12594388 Dysphonia
125943882 12594388 Herpes zoster
125943882 12594388 Nerve injury
125943882 12594388 Pain
125943882 12594388 Treatment noncompliance
125943882 12594388 Weight decreased

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
125943882 12594388 2 1996 0
125943882 12594388 3 2011 0