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What Is Ultram
Ultram (tramadol) is a pain reliever (analgesic) used to treat moderate to moderately severe pain in adults. Ultram is available as 50 mg oral tablets. Ultram is available in generic form.
What Are Side Effects of Ultram?
Side effects of Ultram include: agitation, nervousness, anxiety, seizures (convulsions), skin rash, dizziness, spinning sensation, hallucinations, fever, fast heart rate, overactive reflexes, nausea, vomiting, upset stomach, diarrhea, constipation, loss of coordination, headache, drowsiness, and fainting. Dosage for Ultram Good pain management practice dictates that the dose of Ultram be individualized according to patient need using the lowest beneficial dose.
What Drugs, Substances, or Supplements Interact with Ultram?
Ultram may interact with other drugs including monoamine oxidase inhibitors (MAOIs) and other antidepressant medications. Ultram During Pregnancy and Breastfeeding There are no adequate and well-controlled studies of Ultram in pregnant women. Ultram should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. Ultram passes into breast milk and may harm a nursing baby. Breastfeeding while taking Ultram is not recommended.
Additional Information
Our Ultram Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication. This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. Ultram Professional Information SIDE EFFECTS The following serious adverse reactions are described, or described in greater detail, in other sections: Addiction, Abuse, and Misuse Life-Threatening Respiratory Depression Ultra-Rapid Metabolism of Tramadol and Other Risk Factors for Life-threatening Respiratory Depression in Children Neonatal Opioid Withdrawal Syndrome Interactions with Benzodiazepines or Other CNS Depressants Serotonin Syndrome Seizures Suicide Adrenal Insufficiency Severe Hypotension Gastrointestinal Adverse Reactions Hypersensitivity Reactions Withdrawal Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.
ULTRAM was administered to 550 patients during the double-blind or open-label extension periods in U.S. studies of chronic nonmalignant pain. Of these patients, 375 were 65 years old or older. Table 1 reports the cumulative incidence rate of adverse reactions by 7, 30 and 90 days for the most frequent reactions (5% or more by 7 days). The most frequently reported events were in the central nervous system and gastrointestinal system. Although the reactions listed in the table are felt to be probably related to ULTRAM administration, the reported rates also include some events that may have been due to underlying disease or concomitant medication. The overall incidence rates of adverse experiences in these trials were similar for ULTRAM and the active control groups, TYLENOL with Codeine #3 (acetaminophen 300 mg with codeine phosphate 30 mg), and aspirin 325 mg with codeine phosphate 30 mg, however, the rates of withdrawals due to adverse events appeared to be higher in the ULTRAM groups.
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