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
127663371 12766337 1 I 201202 20160912 20160921 20160921 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-59905BP BOEHRINGER INGELHEIM 71.92 YR F Y 0.00000 20160921 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
127663371 12766337 1 PS COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Respiratory (inhalation) DOSE PER APPLICATION: 20MCG / 100MCG; DAILY DOSE: 80MCG / 400MCG; FORMULATION: INHALATION SPRAY 21747 PRESSURISED INHALATION QID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127663371 12766337 1 Chronic obstructive pulmonary disease

Outcome of event

Event ID CASEID OUTC COD
127663371 12766337 OT
127663371 12766337 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127663371 12766337 Brain injury
127663371 12766337 Cerebrovascular accident
127663371 12766337 Contusion
127663371 12766337 Decreased appetite
127663371 12766337 Dehydration
127663371 12766337 Memory impairment
127663371 12766337 Respiratory arrest
127663371 12766337 Seizure
127663371 12766337 Vein rupture
127663371 12766337 Vomiting

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

no results found

Therapies reported

no results found