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What the label lists and what reports show

Methocarbamol side effects

Methocarbamol's FDA label lists its adverse reactions in its own words. FAERS holds 22,591 reports naming it through July 30, 2026; the reaction reported most often, leaving out the conditions it is used for, product-use terms and outcomes, is pain (1,731 reports).

  • Generic listed

Check it at the source: the methocarbamol FDA label on DailyMed (effective March 17, 2026, Oxford Pharmaceuticals, LLC); the FDA FAERS public dashboard.

What does the label list?

From the label: adverse reactions

Adverse reactions reported coincident with the administration of methocarbamol include: Body as a whole: Anaphylactic reaction, angioneurotic edema, fever, headache Cardiovascular system: Bradycardia, flushing, hypotension, syncope, thrombophlebitis Digestive system: Dyspepsia, jaundice (including cholestatic jaundice), nausea and vomiting Hemic and lymphatic system: Leukopenia Immune system: Hypersensitivity reactions Nervous system: Amnesia, confusion, diplopia, dizziness or lightheadedness, drowsiness, insomnia, mild muscular incoordination, nystagmus, sedation, seizures (including grand mal), vertigo Skin and special senses: Blurred vision, conjunctivitis, nasal congestion, metallic taste, pruritus, rash, urticaria

Source: FDA drug label, Oxford Pharmaceuticals, LLC, effective March 17, 2026 (SPL set 06dc72a6-ef3a-425a-9194-a9d228093cc4), via openFDA; the full label on DailyMed

What do FAERS reports show?

22,591 reports list methocarbamol among the medicines taken, each a report of something that happened, not proof the medicine caused it; 1,740 are coded as a death and 6,803 as a hospital stay. Counts follow how widely a medicine is used and watched, and they are not a measure of how risky it is. Of the 22 reactions below, 6 are named by the same term (in US spelling) in the label's adverse reactions, warnings or patient leaflet; a reaction the label does not name may still be there under another word, and a report does not show that the medicine caused it.

Reports received each year

The 25 most reported reactions

Source: FDA Adverse Event Reporting System (FAERS) via openFDA, reports through July 30, 2026; reactions as MedDRA preferred terms

What next?

Methocarbamol: the full record
label, generics, price, shortages, recalls
Side effects hub
the most reported medicines and reactions