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hydrocodone/chlorpheniramine/phenylephrine (Histussin)

 

Classes: Antitussives, Narcotic Combos

Dosing and uses of Histussin (hydrocodone/chlorpheniramine/phenylephrine)

 

Adult dosage forms and strengths

hydrocodone/chlorpheniramine/phenylephrine

oral liquid: Schedule III

  • (2.5mg/2mg/5mg)/5mL
  • (2.5mg/4mg/10mg)/5mL
  • (3.25mg/2.5mg/8mg)/5mL
  • (3.5mg/4mg/10mg)/5mL
  • (5mg/3mg/7.5mg)/5mL
  • (6mg/2mg/5mg)/5mL
  • (6mg/2mg/12mg)/5mL
  • (10mg/12mg/30mg)/5mL

 

Cough with Congestion

Temporary relief of nasal congestion and cough associated with respiratory tract infections and related conditions

5-10 mL PO q4-6hr PRN, not to exceed maximum dosage limits

Recommended maximum dosage limits

  • Hydrocodone: 30 mg PO in 24 hr
  • Chlorpheniramine: 24 mg PO in 24 hr
  • Phenylephrine: 60 mg PO in 24 hr

 

Other Information

Administer with special measuring device for accurate dose

Administer with food if GI upset occurs

Use caution when dosing due to multiple strengths available

 

Pediatric dosage forms and strengths

hydrocodone/chlorpheniramine/phenylephrine

oral liquid: Schedule III

  • (2.5mg/2mg/5mg)/5mL
  • (2.5mg/4mg/10mg)/5mL
  • (3.25mg/2.5mg/8mg)/5mL
  • (3.5mg/4mg/10mg)/5mL
  • (5mg/3mg/7.5mg)/5mL
  • (6mg/2mg/5mg)/5mL
  • (6mg/2mg/12mg)/5mL
  • (10mg/12mg/30mg)/5mL

 

Cough with Congestion

<6 years: safety and efficacy not established

6-12 years: 2.5-5 mL PO q4-6hr PRN, not to exceed maximum dosage limits

6-12 years: Recommended maximum dosage limits

  • Hydrocodone: 0.6 mg/kg PO, up to 20 mg in 24 hr
  • Chlorpheniramine: 12 mg PO in 24 hr
  • Phenylephrine: 30mg PO in 24 hr

 

Histussin (hydrocodone/chlorpheniramine/phenylephrine) adverse (side) effects

Frequency not defined

Hydrocodone

  • Bradycardia, anticholinergic effects (dry mouth, palpitation, tachycardia)
  • Angina, arrhythmias, cardiac arrest, myocardial infarction, QT-interval prolongation, pectoris, syncope, severe cardiac ST segment elevation, ventricular tachycardia
  • Agitation, coma, dizziness, mental clouding/depression, dysphoria, euphoria, faintness, restlessness, nervousness, weakness, sedation, seizures, visual disturbances
  • Flushing, sweating, pruritus, urticaria, warmness of the face/neck/upper thorax
  • Constipation, nausea, vomiting
  • Urinary retention, oliguria
  • Respiratory/circulatory depression, respiratory arrest, shock, cardiac arrest

Chlorpheniramine

  • Anticholinergic side effects
  • Somnolence
  • Constipation, diarrhea, nausea, vomiting
  • Blurred vision

Phenylephrine

  • Hypertension, reflex bardycardia
  • Anxiety, headache
  • Extravasation
  • Burning, rebound congestion, sneezing
  • Pulmonary edema

 

Warnings

Contraindications

Hydrocodone

  • Absolute: acute abdominal condition, diarrhea associated with toxins, paralytic ileus, pseudomembranous colitis, respiratory depression
  • Relative: asthma (acute), cardiac arrhythmia, cardiac disease, congestive heart failure, coronary artery DX, bladder outlet obstruction, GI tract obstruction, glaucoma (open & closed), hemorrhage, hiatal hernia, inflammatory bowel disease, intestinal atony, mitral valve stenosis, myasthenia gravis, obstructive uropathy, prostatic hypertrophy, reflux esophagitis, respiratory impairment, tachycardia, ulcerative colitis, urinary retention

Chlorpheniramine

  • Acute asthma, sleep apnea

Phenylephrine

  • Hypersensitivity to phenylephrine or sulfites; severe HTN, VTach, closed angle glaucoma
  • See Interactions below

 

Pregnancy and lactation

Pregnancy category: C

Lactation: hydrocodone, chlorpheniramine and phenylephrine excreted into breast milk; nursing not recommended

 

Pregnancy categories

A: Generally acceptable. Controlled studies in pregnant women show no evidence of fetal risk.

B: May be acceptable. Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk.

C: Use with caution if benefits outweigh risks. Animal studies show risk and human studies not available or neither animal nor human studies done.

D: Use in LIFE-THREATENING emergencies when no safer drug available. Positive evidence of human fetal risk.

X: Do not use in pregnancy. Risks involved outweigh potential benefits. Safer alternatives exist.

NA: Information not available.

 

Pharmacology of Histussin (hydrocodone/chlorpheniramine/phenylephrine)

Hydrocodone

Half-life: 3.3-4.4 hr

Duration: 4-8 hr

Peak PlasmaTime: 1.3 hr

Metabolism: liver (O-demethylation, N-demethylation, 6-keto reduction); hepatic P450 enzyme CYP2D6

Excretion: urine (mainly)

 

Chlorpheniramine

Half-Life: 12-43 hr

Duration: 24 hr

Onset: 6 hr

Peak Plasma Time: 2-6 hr

Protein Bound: 69-72%

Vd: 2.5-3.2 L/kg

Metabolism: GI mucosa, liver

Metabolites: monodesmethylchlorpheniramine, didesmethylchlorpheniramine

Excretion: urine

Sedative effect: low

Antihistamine activity: moderate

Anticholinergic acitivity: moderate

 

Phenylephrine

Duration: 2-4 hr

Onset: 15-20 min

Metabolism: liver & intestine by MAO

Excretion: urine