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:: Overview :: Precautions :: Side Effects Search results last updated: 9/16/2008

Generic & Brand Name : Source: (MedicineNet)

Brand Name : Broncomar GG, Quibron, Slo-Phyllin GG, Theomar GG
Generic Name : GUAIFENESIN WITH THEOPHYLLINE - ORAL (gweye-FEN-eh-sin WITH thee-OFF-ih-lin)

Overview (Source: MedicineNet)
Topics Related to guaifenesin with theophylline-oral, Broncomar GG, Quibron, Slo-Phyllin GG, Theomar GG ...
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Precautions (Source: MedLinePlus)
Before taking guaifenesin, tell your doctor and pharmacist if you are allergic to guaifenesin, any other medications, or any of the ingredients in the guaifenesin product you plan to take. Check the package label for a list of the ingredients. tell your doctor and pharmacist what prescription and nonprescription medications, vitamins, nutritional supplements, and herbal products you are taking or plan to take. tell your doctor if you smoke and if you have or have ever had a cough that occurs with a large amount of phlegm (mucus) or if you have or have ever had a breathing problem such as asthma, emphysema, or chronic bronchitis. If you will be taking the dissolving granules, tell your doctor if you are on a low magnesium diet or if you have kidney disease. tell your doctor if you are pregnant, plan to become pregnant, or are breast-feeding. If you become pregnant while taking guaifenesin, call your doctor. if you have phenylketonuria (PKU, a inherited condition in which a special diet must be followed to prevent mental retardation), you should know that the dissolving granules may be sweetened with aspartame, a source of phenylalanine. ...
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Side Effects (Source: MedLinePlus)
Guaifenesin may cause side effects. Tell your doctor if any of these symptoms are severe or do not go away: headache; nausea; vomiting. Guaifenesin may cause other side effects. Call your doctor if you have any unusual problems while you are taking this medication. If you experience a serious side effect, you or your doctor may send a report to the Food and Drug Administration's (FDA) MedWatch Adverse Event Reporting program online [at http://www.fda.gov/MedWatch/index.html ] or by phone [1-800-332-1088]. ...
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