Drug adverse event reports (FAERS)

Cardio-respiratory arrest, Choking, Aspiration

Drugs: CARBIDOPA\LEVODOPA

SeriousDeathReport 27325193
Safetyreportversion
1
Safetyreportid
27325193
Primarysourcecountry
EU
Occurcountry
EU
Transmissiondateformat
102
Transmissiondate
20261010
Reporttype
2
Serious
1
Seriousnessdeath
1
Seriousnesslifethreatening
2
Seriousnesshospitalization
2
Seriousnessdisabling
2
Seriousnesscongenitalanomali
2
Seriousnessother
2
Receivedateformat
102
Receivedate
20260930
Receiptdateformat
102
Receiptdate
20260930
Fulfillexpeditecriteria
1
Companynumb
EU-ABBVIE-6956196
Primarysource
Reportercountry
EU
Qualification
5
Sender
Sendertype
6
Senderorganization
ABBVIE
Receiver
Receivertype
6
Receiverorganization
FDA
Patient
Patientonsetage
72
Patientonsetageunit
801
Patientsex
1
Reaction
  1. Reactionmeddraversionpt
    29.0
    Reactionmeddrapt
    Cardio-respiratory arrest
    Reactionoutcome
    5
  2. Reactionmeddraversionpt
    29.0
    Reactionmeddrapt
    Choking
    Reactionoutcome
    5
  3. Reactionmeddraversionpt
    29.0
    Reactionmeddrapt
    Aspiration
    Reactionoutcome
    5
Drug
  1. Drugcharacterization
    1
    Medicinalproduct
    CARBIDOPA\LEVODOPA
    Drugbatchnumb
    Not available
    Drugauthorizationnumb
    203952
    Drugseparatedosagenumb
    1
    Drugindication
    Parkinson^s disease
    Drugstartdateformat
    102
    Drugstartdate
    20250309
    Drugenddateformat
    102
    Drugenddate
    20260928
    Drugtreatmentduration
    18
    Drugtreatmentdurationunit
    802
    Actiondrug
    6
    Drugadditional
    4
    Activesubstance
    Activesubstancename
    CARBIDOPA\LEVODOPA
  2. Drugcharacterization
    1
    Medicinalproduct
    CARBIDOPA\LEVODOPA
    Drugauthorizationnumb
    203952
    Actiondrug
    6
    Drugadditional
    4
    Activesubstance
    Activesubstancename
    CARBIDOPA\LEVODOPA
Summary
Narrativeincludeclinical
CASE EVENT DATE: 20260928
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How to read this: Each report says someone told FDA an event happened while a product was used. A report does not show the product caused it, and counts rise and fall with how many people report. Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.