Carbiset Side Effects
Generic name: carbinoxamine / pseudoephedrine
Note: This document provides detailed information about Carbiset Side Effects associated with carbinoxamine / pseudoephedrine. Some dosage forms listed on this page may not apply specifically to the brand name Carbiset.
Applies to carbinoxamine/pseudoephedrine: oral liquid, oral suspension extended release, oral tablet, oral tablet chewable, oral tablet extended release.
Important warnings
This medicine can cause some serious health issues
Always ask a doctor before giving a cold or allergy medicine to a child, even if the medicine label provides dosing instructions for children. Death can occur from the misuse of cough and cold medicines in very young children.
Do not use carbinoxamine and pseudoephedrine if you have used an MAO inhibitor such as isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam), or tranylcypromine (Parnate) within the past 14 days. Serious, life-threatening side effects can occur if you take carbinoxamine and pseudoephedrine before the MAO inhibitor has cleared from your body.
Carbinoxamine and pseudoephedrine can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert.
Avoid drinking alcohol. It can increase some of the side effects of this medication.
Call your doctor if you have a fever, or if your symptoms get worse or do not improve after taking this medicine for 7 days.
Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.
Stop using this medication and call your doctor at once if you have any of these serious side effects:
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feeling light-headed, fainting;
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urinating less than usual or not at all;
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wheezing, tightness in your chest;
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severe dizziness, anxiety, restless feeling, or nervousness;
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easy bruising or bleeding, unusual weakness, fever, chills, body aches, flu symptoms; or
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increased blood pressure (severe headache, blurred vision, trouble concentrating, chest pain, numbness, seizure).
Continue taking this medication and talk to your doctor if you have any of these less serious side effects:
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drowsiness, dizziness;
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lack of coordination;
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stuffy nose, chest congestion;
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sleep problems (insomnia);
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feeling restless or excited (especially in children);
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dry mouth or nose; or
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blurred vision.
Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.
For healthcare professionals
Applies to carbinoxamine / pseudoephedrine: oral liquid, oral suspension extended release, oral tablet, oral tablet chewable, oral tablet extended release.
General
General side effects have included weakness and pallor.[Ref]
Gastrointestinal
Gastrointestinal side effects have included vomiting, diarrhea, dry mouth, nausea, anorexia, and heart burn.[Ref]
Cardiovascular
Cardiovascular side effects have included arrhythmias and increased heart rate or blood pressure.[Ref]
Genitourinary
Genitourinary side effects have included polyuria and dysuria.[Ref]
Nervous system
Nervous system side effects have included sedation, dizziness, headache, nervousness, convulsion, central nervous system stimulation, tremors, hallucinations, and insomnia.[Ref]
Ocular
Ocular side effects have included diplopia.[Ref]
Respiratory
Respiratory side effects have included respiratory difficulty.[Ref]
References
1. (2004) "Product Information. Pediatex D (carbinoxamine-pseudoephedrine)." Zyber Pharmaceuticals Inc
More about Carbiset (carbinoxamine / pseudoephedrine)
- Check interactions
- Compare alternatives
- Dosage information
- During pregnancy
- Drug class: upper respiratory combinations
Related treatment guides
Further information
Carbiset side effects can vary depending on the individual. 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.