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
105875031 10587503 1 I 20141026 20141106 20141117 20141117 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2014-BI-53617BP BOEHRINGER INGELHEIM 79.59 YR F Y 83.91000 KG 20141117 N CN 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
105875031 10587503 1 PS SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 INHALATION 18 MCG D 404428A,14C3206 21395 18 UG INHALATION POWDER, HARD CAPSULE QD
105875031 10587503 2 C COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 INHALATION DOSE PER APPLICATION: 20 MCG / 400 MCG; DAILY DOSE: 80 MCG / 400 MCG D 0 PRESSURISED INHALATION QID
105875031 10587503 3 C NORVASC AMLODIPINE BESYLATE 1 ORAL 7.5 MG D 0 7.5 MG TABLET QD
105875031 10587503 4 C DIOVAN VALSARTAN 1 ORAL 20 MG D 0 20 MG TABLET QD
105875031 10587503 5 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 ORAL 10 MG D 0 10 MG CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105875031 10587503 1 Emphysema
105875031 10587503 2 Emphysema
105875031 10587503 3 Hypertension
105875031 10587503 4 Hypertension
105875031 10587503 5 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
105875031 10587503 Chest discomfort
105875031 10587503 Dysphonia
105875031 10587503 Oropharyngeal pain

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
105875031 10587503 1 20141015 20141026 0
105875031 10587503 2 2013 201410 0