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Butalbital/Aspirin/Caffeine/Codeine/

    DEA Class;  Rx, schedule III

    Common Brand Names; Fiorinal with Codeine 

    Analgesic and opioids combos

    Salicylate analgesic (aspirin), short-to-intermediate acting barbiturate (butalbital), CNS stimulant (caffeine), and opiate agonist (codeine)

    Used together to treat mild to moderate pain and headaches, especially when antianxiety or relaxant effects are needed

    Codeine metabolism is highly variable and unpredictable; use in patients younger than 12 years is contraindicated

    Indicated For the treatment of occasional tension headache, occasional migraine† or co-existing migraine† and tension-type headaches.

    Hypersensitivity

    Children <12 years (increased risk of death from opioid)

    Postoperative management in children <18 years following tonsillectomy and/or adenoidectomy

    Children <16 years because of potential for Reye syndrome

    Postoperative use in children following tonsillectomy and/or adenoidectomy 

    Bronchospastic reaction to aspirin

    Syndrome of asthma, rhinitis, and nasal polyps

    Significant respiratory depression

    Peptic ulcer disease

    Known allergy to NSAIDs

    Within 14 days of taking MAOIs

    Hemophilia

    Repeated administration in patients with anemia, cardiovascular, pulmonary, or renal disease

    Porphyria

    >10%

    Codeine

    Constipation

    Drowsiness

    1-10%

    Codeine

    Hypotension, tachycardia or bradycardia, confusion, dizziness, false feeling of well being, headache, lightheadedness, malaise, paradoxical CNS stimulation, restlessness, rash, urticaria, anorexia, nausea, vomiting, xerostomia, ureteral spasm, urination decreased, LFT’s increased, weakness, blurred vision, dyspnea, histamine-release

     

    Butalbital

    Dizziness, drowsiness, feeling of intoxication, lightheadedness, sedation

    Abdominal pain, nausea, vomiting

    Shortness of breath

    Aspirin

    Dyspepsia, heartburn, nausea, vomiting, stomach pain

    Tinnitus (high or chronic dose)

    Rash

    Urticaria

    Caffeine

    Tachycardia, palpitations (dose dependent)

    Insomnia, irritability, nervousness, restlessness, tinnitus, tremor

    Diarrhea, nausea, vomiting

    Diuresis

    Particular caution in patients with history of GI bleed, alcoholism, or bleeding disorders

    Avoid driving car or operating machinery

    Avoid in severe renal impairment (ie, CrCl <10 mL/min)

    Avoid use of mixed agonist/antagonist (eg, pentazocine, nalbuphine, and butorphanol) or partial agonist (eg, buprenorphine) analgesics in patients who are receiving a full opioid agonist analgesic; mixed agonist/antagonist and partial agonist analgesics may reduce the analgesic effect and/or precipitate withdrawal symptoms

    May increase respiratory depressant effects; caution with head injury, COPD, or other conditions with decreased respiratory drive

    As butalbital, aspirin, caffeine, and codeine phosphate drug dosage forms contain butalbital and codeine, they expose users to the risks of addiction, abuse, and misuse; assess each patient’s risk for addiction, abuse, or misuse prior to prescribing therapy, and monitor all patients receiving drug for development of addiction behaviors and conditions

    Pregnancy

    Prolonged use of opioid analgesics during pregnancy may cause neonatal opioid withdrawal syndrome; available data in pregnant women are insufficient to inform a drug-associated risk for major birth defects and miscarriage

    Withdrawal seizures reported in two-day-old male infant whose mother had taken a butalbital-containing drug during the last 2 months of pregnancy; butalbital was found in infant’s serum; the infant was given phenobarbital 5 mg/kg, which was tapered without further seizure or other withdrawal symptoms

    Lactation: Codeine and its active metabolite, morphine, are present in human milk; there are published studies and cases that have reported excessive sedation, respiratory depression, and death in infants exposed to codeine via breast milk; women who are ultra-rapid metabolizers of codeine achieve higher than expected serum levels of morphine, potentially leading to higher levels of morphine in breast milk that can be dangerous in their breastfed infants; in women with normal codeine metabolism (normal CYP2D6 activity), the amount of codeine secreted into human milk is low and dose-dependent

    Adults

    6 capsules/day PO.

    Geriatric

    6 capsules/day PO.

    Adolescents

    Safety and efficacy have not been established.

    Children

    12 years: Safety and efficacy have not been established.

    1 to 11 years: Use is contraindicated.

    Infants

    Use is contraindicated.

    butalbital/aspirin/caffeine/codeine

    Capsule: Schedule III

    50mg/325mg/40mg/30mg