White tablet 377

The pill is an elliptical or oval-shaped, white-colored tablet with an imprint of "".

If you are a consumer or patient please visit this version. Tramadol hydrochloride tablet, USP is a centrally acting analgesic. Its structural formula is:. The molecular weight of tramadol hydrochloride, USP is Tramadol hydrochloride, USP is a white, bitter, crystalline and odorless powder. It is readily soluble in water and ethanol and has a pKa of 9.

White tablet 377

Tramadol is a prescription medication used to treat moderate to moderately severe pain in adults. Tramadol belongs to a group of drugs called opioid analgesics, which work by blocking pain signals in the body. This medication comes in immediate release tablet and that can be taken up to 6 times a day, with or without food. Tramadol also comes in extended-release tablet and capsule forms and are taken once a day, with or without food. Do not chew, divide, or break tramadol extended-release forms. Swallow them whole. Common side effects of tramadol include nausea, constipation, dry mouth, and fatigue. Tramadol can also cause dizziness or drowsiness. Do not drive or operate heavy machinery until you know how tramadol affects you. CYP2D6 is a protein in your body that is involved in the elimination of tramadol and other drugs from your body. Some patients have more or less of this protein in their bodies, affecting how much of the drug gets eliminated. Levels of CYP2D6 can vary greatly between individuals, and those having less of this protein are known as "poor metabolizers.

Chronic use during pregnancy may lead to physical dependence and post-partum withdrawal symptoms in the newborn.

If you are a consumer or patient please visit this version. Dosage and Administration 2. Warnings and Precautions 5. Tramadol hydrochloride tablets are an opioid agonist indicated in adults for the management of pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate 1. Limitations of Use 1.

Mary's Medical Park Pharmacy. Tramadol hydrochloride tablet, USP is a centrally acting analgesic. Its structural formula is:. The molecular weight of tramadol hydrochloride, USP is Tramadol hydrochloride, USP is a white, bitter, crystalline and odorless powder. It is readily soluble in water and ethanol and has a pKa of 9. In addition, each tablet contains the following inactive ingredients: pregelatinized starch, lactose anhydrous, magnesium stearate, microcrystalline cellulose, polyethylene glycol, sodium starch glycolate, titanium dioxide, hypromellose and polysorbate Tramadol hydrochloride is a centrally acting synthetic opioid analgesic. Tramadol-induced analgesia is only partially antagonized by the opiate antagonist naloxone in several animal tests.

White tablet 377

If you are a consumer or patient please visit this version. Dosage and Administration 2. Warnings and Precautions 5. Tramadol hydrochloride tablets are an opioid agonist indicated in adults for the management of pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate 1. Limitations of Use 1. Because of the risks of addiction, abuse, and misuse with opioids, which can occur at any dosage or duration, reserve tramadol hydrochloride tablets for use in patients for whom alternative treatment options [e. Life-Threatening Respiratory Depression. Serious, life-threatening, or fatal respiratory depression may occur with use of tramadol hydrochloride tablets, especially during initiation or following a dosage increase.

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Constipation Advise patients of the potential for severe constipation, including management instructions and when to seek medical attention [see Adverse Reactions 6 ]. Cardiac arrest or arrhythmias may require cardiac massage or defibrillation. There is no evidence of self-induction see Figure 1 and Table 1 below. When discontinuing tramadol hydrochloride tablets in a physically dependent patient, gradually taper the dosage. It is usually given after an individual has undergone surgery or an accident. The judicious prescribing of tramadol is essential to the safe use of this drug. Although the risk of addiction in any individual is unknown, it can occur in patients appropriately prescribed tramadol hydrochloride tablets. These dosages are 1. Tramadol Cautionary Labels Back to Top. If one is not available, you can dispose of tramadol hydrochloride tablets by mixing the product with dirt, cat litter, or coffee grounds; placing the mixture in a sealed plastic bag, and throwing the bag in your trash. Your doctor may adjust your dose of tramadol if you are a poor metabolizer. In patients who may be susceptible to the intracranial effects of CO 2 retention e. If naloxone is prescribed, educate patients and caregivers on how to treat with naloxone. Evaluate patients for signs of urinary retention or reduced gastric motility when tramadol hydrochloride tablets are used concomitantly with anticholinergic drugs.

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Below are the other types of pain, which can be treated with the help of the pill:. Patients with a variety of chronic painful conditions were studied in double-blind trials of one to three months duration. Misuse is the intentional use, for therapeutic purposes, of a drug by an individual in a way other than prescribed by a health care provider or for whom it was not prescribed. In subjects over 75 years, maximum serum concentrations are elevated vs. Approval: This information does not replace the advice of a doctor. Since tramadol is used for pain, you are not likely to miss a dose. Opioids are sought for nonmedical use and are subject to diversion from legitimate prescribed use. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. Intervention: If concomitant use is warranted, frequently evaluate the patient, particularly during treatment initiation and dose adjustment. Version Files Aug 22, 1 current download. Healthy elderly subjects aged 65 to 75 years have plasma tramadol concentrations and elimination half-lives comparable to those observed in healthy subjects less than 65 years of age. Monitor such patients for signs of sedation and respiratory depression, particularly when initiating therapy with tramadol hydrochloride tablets.