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guaifenesin Anti-Tuss, Balminil Expectorant ◆, Breonesin, Diabetic Tussin EX, Duratuss-G Fenesin, Gee-Gee, Genatuss, GG-Cen, Glyate, Glycotuss, Glytuss, Guafenex LA, Humibid LA, Humibid Sprinkle, Hytuss, Hytuss 2X, Mucinex, Muco-Fen-LA, Mytussin, Naldecon Senior EX, Organidin NR, Respa-GF, Resyl ◆, Robitussin, Scot-Tussin, Touro EX, Tusibron, Uni-tussin
Pharmacologic classification: propanediol derivative Therapeutic classification: expectorant Pregnancy risk category C
Available forms Available by prescription only Capsules: 300 mg Tablets: 1,200 mg Tablets (extended-release): 600 mg, 1,200 mg Capsules: 200 mg Capsules (extended-release): 300 mg Syrup: 100 mg/5 ml, 200 mg/5 ml Tablets: 100 mg, 200 mg Tablets (extended-release): 600 mg
Indications and dosages
Expectorant. Adults and children age 12 and older: 100 to 400 mg P.O. q 4 hours. Maximum, 2.4 g daily. Children ages 6 to 11: 100 to 200 mg P.O. q 4 hours. Maximum, 1.2 g daily. Children ages 2 to 5: 50 to 100 mg P.O. q 4 hours. Maximum, 600 mg daily. Children younger than age 2: Individualize dosage. Extended-release form Adults and children older than age 12: 600 to 1,200 mg P.O. q 12 hours. Maximum, 2,400 mg in 24 hours. Children ages 6 to 12: 600 mg P.O. q 12 hours. Maximum, 1,200 mg in 24 hours. Children ages 2 to 6: 300 mg P.O. q 12 hours. Maximum, 600 mg in 24 hours.
Pharmacodynamics Expectorant action: Guaifenesin increases respiratory tract fluid by reducing adhesiveness and surface tension, decreasing viscosity of the secretions
and thereby facilitating their removal.
Pharmacokinetics Absorption: Unknown.
| Route |
Onset |
Peak |
Duration |
| P.O. |
Unknown |
Unknown |
Unknown |
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Contraindications and precautions Contraindicated in patients hypersensitive to drug.
Interactions None significant.
Adverse reactions CNS: dizziness, headache. GI: vomiting, nausea (with large doses). Skin: rash.
Effects on lab test results None reported.
Overdose and treatment No information available.
Special considerations Efficacy of guaifenesin as an expectorant hasn’t been clearly established because of conflicting results of clinical studies.
Reevaluate patient if symptoms persist for longer than 1 week, if cough recurs, or if cough is accompanied by fever, rash,
or persistent headache. Breast-feeding patients It isn’t known whether drug appears in breast milk. Safety in breast-feeding women hasn’t been established. Pediatric patients Individualize dosage for children younger than age 2. Geriatric patients No specific recommendations are available. Most liquid forms contain alcohol (3.5% to 10%).
Patient education Advise patient to take drug with a glass of water to help loosen mucus in lungs. Advise patient to use sugarless throat lozenges to decrease throat irritation and cough and to report cough that persists
longer than 7 days.
Reactions may be common, uncommon, life-threatening, or
COMMON AND LIFE THREATENING.
◆ Canada only
◇ Unlabeled clinical use
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