Dolitabs Side Effects
Generic name: acetaminophen
Medically reviewed by Drugs.com. Last updated on Dec 23, 2022.
Note: This document contains side effect information about acetaminophen. Some dosage forms listed on this page may not apply to the brand name Dolitabs.
Applies to acetaminophen: capsule, capsule liquid filled, elixir, liquid, powder, solution, suppository, suspension, tablet, tablet chewable, tablet disintegrating, tablet extended release. Other dosage forms:
Serious side effects of Dolitabs
Along with its needed effects, acetaminophen (the active ingredient contained in Dolitabs) may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.
Check with your doctor immediately if any of the following side effects occur while taking acetaminophen:
- Bloody or black, tarry stools
- bloody or cloudy urine
- fever with or without chills (not present before treatment and not caused by the condition being treated)
- pain in the lower back and/or side (severe and/or sharp)
- pinpoint red spots on the skin
- skin rash, hives, or itching
- sore throat (not present before treatment and not caused by the condition being treated)
- sores, ulcers, or white spots on the lips or in the mouth
- sudden decrease in the amount of urine
- unusual bleeding or bruising
- unusual tiredness or weakness
- yellow eyes or skin
Get emergency help immediately if any of the following symptoms of overdose occur while taking acetaminophen:
Symptoms of overdose
- increased sweating
- loss of appetite
- nausea or vomiting
- stomach cramps or pain
- swelling, pain, or tenderness in the upper abdomen or stomach area
For Healthcare Professionals
Applies to acetaminophen: compounding powder, intravenous solution, oral capsule, oral granule effervescent, oral liquid, oral powder, oral powder for reconstitution, oral suspension, oral tablet, oral tablet chewable, oral tablet disintegrating, oral tablet extended release, rectal suppository.
In general, acetaminophen (the active ingredient contained in Dolitabs) is well-tolerated when administered in therapeutic doses. The most commonly reported adverse reactions have included nausea, vomiting, constipation. Injection site pain and injection site reaction have been reported with the IV product.[Ref]
Common (1% to 10%): Increased aspartate aminotransferase
Rare (less than 0.1%): Increased hepatic transaminases
Frequency not reported: Liver failure[Ref]
Very common (10% or more): Nausea (up to 34%), Vomiting (up to 15%)
Frequency not reported: Dry mouth[Ref]
Common (1% to 10%): Anemia, postoperative hemorrhage
Common (1% to 10%): Rash, pruritus
Very rare (less than 0.01%): Pemphigoid reaction, pustular rash, Lyell syndrome[Ref]
Common (1% to 10%): Headache, dizziness
Frequency not reported: Dystonia
Common (1% to 10%): Muscle spasms, trismus
Common (1% to 10%): Oliguria
Common (1% to 10%): Infusion site pain, injection site reactions
Common (1% to 10%): Periorbital edema
Common (1% to 10%): Pyrexia, fatigue
Rare (0.01% to 0.1%): Malaise
Frequently asked questions
- What's the best sore throat medicine to use?
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- What is paracetamol / panadol called in the US?
- Advil (ibuprofen) & Tylenol (acetaminophen) together, is it safe?
- How long does it take for Tylenol to start working?
- Can you take tramadol with acetaminophen, ibuprofen, or aspirin?
- Is it safe to take acetaminophen every day?
- Is acetaminophen the same as Tylenol?
- Is Tylenol (acetaminophen) a blood thinner?
- Is acetaminophen (Tylenol) an NSAID Drug?
- Is Tylenol (acetaminophen) an anti-inflammatory drug?
- Can you take paracetamol (acetaminophen) with antibiotics?
- Can I give my dog or cat Tylenol (acetaminophen)?
More about Dolitabs (acetaminophen)
- Check interactions
- Latest FDA alerts (16)
- Dosage information
- During pregnancy
- Drug class: miscellaneous analgesics
Related treatment guides
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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.