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
126266501 12626650 1 I 201602 20160725 20160805 20160805 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-48905BP BOEHRINGER INGELHEIM 52.19 YR F Y 0.00000 20160805 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
126266501 12626650 1 PS COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Respiratory (inhalation) 8 ANZ Y 21747 PRESSURISED INHALATION QID
126266501 12626650 2 SS COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Respiratory (inhalation) 4 ANZ Y 21747 PRESSURISED INHALATION QID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126266501 12626650 1 Chronic obstructive pulmonary disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126266501 12626650 Dyspepsia
126266501 12626650 Incorrect dosage administered
126266501 12626650 Memory impairment
126266501 12626650 Stomatitis

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
126266501 12626650 1 201602 201602 0
126266501 12626650 2 201602 0