Drug adverse event reports (FAERS)

Suicidal ideation, Fatigue, Illness +2

Drugs: ARMOUR THYROID

SeriousOther seriousReport 27325240
Safetyreportversion
1
Safetyreportid
27325240
Primarysourcecountry
US
Occurcountry
US
Transmissiondateformat
102
Transmissiondate
20261010
Reporttype
2
Serious
1
Seriousnessdeath
2
Seriousnesslifethreatening
2
Seriousnesshospitalization
2
Seriousnessdisabling
2
Seriousnesscongenitalanomali
2
Seriousnessother
1
Receivedateformat
102
Receivedate
20260930
Receiptdateformat
102
Receiptdate
20260930
Fulfillexpeditecriteria
1
Companynumb
US-ABBVIE-6952949
Primarysource
Reportercountry
US
Qualification
5
Sender
Sendertype
6
Senderorganization
ABBVIE
Receiver
Receivertype
6
Receiverorganization
FDA
Patient
Patientagegroup
6
Patientsex
2
Reaction
  1. Reactionmeddraversionpt
    29.0
    Reactionmeddrapt
    Suicidal ideation
    Reactionoutcome
    6
  2. Reactionmeddraversionpt
    29.0
    Reactionmeddrapt
    Fatigue
    Reactionoutcome
    6
  3. Reactionmeddraversionpt
    29.0
    Reactionmeddrapt
    Illness
    Reactionoutcome
    6
  4. Reactionmeddraversionpt
    29.0
    Reactionmeddrapt
    Gait inability
    Reactionoutcome
    3
  5. Reactionmeddraversionpt
    29.0
    Reactionmeddrapt
    Asthenia
    Reactionoutcome
    6
Drug
  1. Drugcharacterization
    1
    Medicinalproduct
    ARMOUR THYROID
    Drugstructuredosagenumb
    90
    Drugstructuredosageunit
    003
    Drugseparatedosagenumb
    1
    Drugintervaldosageunitnumb
    1
    Drugintervaldosagedefinition
    804
    Drugdosagetext
    FORM STRENGTH: 90 MILLIGRAM
    Drugdosageform
    Tablet
    Drugindication
    Product used for unknown indication
    Actiondrug
    5
    Drugadditional
    3
    Activesubstance
    Activesubstancename
    THYROID, PORCINE
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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.