SymPak II Side Effects
Generic name: brompheniramine / chlorpheniramine / methscopolamine / phenylephrine / pseudoephedrine
Note: This document contains side effect information about brompheniramine / chlorpheniramine / methscopolamine / phenylephrine / pseudoephedrine. Some dosage forms listed on this page may not apply to the brand name SymPak II.
Applies to brompheniramine / chlorpheniramine / methscopolamine / phenylephrine / pseudoephedrine: oral kit.
Do not use this medicine if you have used an MAO inhibitor in the past 14 days, such as isocarboxazid, linezolid, methylene blue injection, phenelzine, rasagiline, selegiline, or tranylcypromine.
You should not use antihistamine medication to make a child sleepy.
Get emergency medical help if you have signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat.
Stop using this medicine and call your doctor at once if you have:
pounding heartbeats or fluttering in your chest;
shortness of breath;
tremor, seizure (convulsions);
ongoing diarrhea or vomiting;
little or no urination;
easy bruising or bleeding, unusual weakness; or
high blood pressure--severe headache, blurred vision, pounding in your neck or ears, nosebleed, anxiety.
Side effects such as dry mouth, constipation, and confusion may be more likely in older adults.
Common side effects may include:
headache, dizziness, drowsiness;
dry mouth, nose, or throat;
nausea, bloating, constipation;
feeling nervous or restless;
sleep problems (insomnia); or
This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects.
More about SymPak II (brompheniramine / chlorpheniramine / methscopolamine / phenylephrine / pseudoephedrine)
- Check interactions
- Compare alternatives
- Dosage information
- Drug class: upper respiratory combinations
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Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
Some side effects may not be reported. You may report them to the FDA.