Robaxin is a muscle relaxant. It is used together with rest and physical therapy to treat skeletal muscle conditions such as pain or injury.

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Robaxin 500mg tablets dosage form has not been evaluated in women of childbearing potential. Children As with adults, the recommended maximum starting dose for children is one capsule twice daily for infants aged 1 buy robaxin canada month to 6 years. See Table 4. For children who are 6 years or older, the dose should be increased gradually to the maximum recommended dosage without undue risk to the Robaxin 500mg $51.09 - $0.57 Per pill child's health and safety. To reduce the risk of adverse reactions, dose the drug may be decreased in increments of 2.5 mg per kg body weight (3.3 mg per 3.3 kg) by 2 to 4 mg per kg of body weight (1.3 to 2.7 mg per 3.3 kg) in children for whom it has not been evaluated and to the maximum tolerated dose in absence of such evaluation. A decrease ≥5% in the maximum dose should be avoided in children for whom it has not been evaluated and to the maximum tolerated dose without undue risk to the child's health. Table 4. Recommended Dose for Children With Dizziness or Abnormal Situations Dosage (mg) Maximum Dose Normal Situation 1 2.5–4 0.2–0.3 3 12–16 0.8–1.0 4 4–6 2.5–4 5–8 3.3–4 6 16–20 7–10 3.4–5 8 20–24 2.5–4 Adults The recommended maximum starting dose for adults aged 19 years and older is 100 robaxin tablets used mg twice daily. However, in the absence of clinical experience demonstrating safety, the dose may be increased to 200 mg twice daily in patients with mild to moderate symptoms. reduce the risk of adverse reactions, dose may be decreased in increments of 5–10 mg 2 to 4 per kg of body weight (3 to 8 mg per 3.3 kg) in men and women. The following table provides an overview of the most common adverse reactions. See Table 5. Table 5. Common Adverse Reactions in Adults with Depression and the General Population Dosage (mg) Headache 4 Dizziness 10 Nausea 5 Vomiting 2 Upset stomach 2 Diarrhea 2 Diarrhea or constipation 2 Drowsiness 2 Fatigue 1 Constipation 1 Generalized tonic-clonic seizures 1 Musculoskeletal pain 1 Muscle cramps or stiffness 1 Dental disease 1 HIV-1 or HIV-2 infection 1 Adverse reactions other than those listed above should be reported to FDA at 1-800-FDA-1088. Laboratory Tests In case of detection the drug in urine or serum, the laboratory should test for presence of co-prescribed drugs. If co-prescription drugs are present, they should be discontinued. If co-prescribed drugs are not detected (i.e., the drug cannot be identified), must discontinued. Patient Counseling Information Advise the patient to read Medication Guide provided by his or her healthcare professional. Patients should be advised to report negative drug test results [see Warnings and Precautions (5.2)] to their healthcare professional immediately. Inform patients that at least 2 weeks of abstinence is required before resuming use. Consult clinical trial information before starting a new medication and each month during treatment [see Clinical Pharmacology (12.3)]. Advise patients to report all new or worsening symptoms, including those that may suggest the need for discontinuation of drug therapy, to their healthcare professional [see Warnings and Precautions (5.3)]. Indications In the treatment of depression, bupropion dimesylate is indicated in the following indications: Patients with major depressive disorder (MDD) resistant to antidepressant monotherapy Patients with MDD who have not responded to at least 2 adequate trials of an antidepressant monotherapy Severely depressed patients Patients with bipolar disorder (manic-depression) Nontreated patients with major depression (MDD) who have failed at least 1 adequate antidepressant trial Patients who are at greater risk for adverse reactions to antidepressants (e.g., patients with a history of suicide, children, patients with a family history of suicide, subjects whose condition is expected to result in an elevated suicide risk, and patients with a comorbid condition such as substance abuse or psychosis) Pediatric Patients Advise pediatric patients receiving bupropion dimesylate to tell their healthcare professional if they have begun or plan to start taking any non-prescription, controlled substance, such.

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