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Therefore, robaxin® and robaxin® -750 should not be used in women who are or may become pregnant and particularly during early pregnancy unless in the judgment of the robaxin physician the potential benefits outweigh the possible hazards (see WARNINGS) .
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Because many drugs are excreted in human milk, caution should be exercised when robaxin® or robaxin® -750 is administered to a nursing Safety and effectiveness of robaxin® and robaxin® -750 in pediatric patients below the age of robaxin 16 have not been established .
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, robaxin 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, Limited information is available on the acute toxicity of methocarbamol .
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