Tramadol is an oral medication that is used to help relieve ongoing moderate to moderately severe pain. Tramadol is similar to opioid (narcotic) analgesics. It works in the brain to change how your body feels and responds to pain.
Tramadol is a narcotic-like pain relieving oral medicine that is used as a treatment for moderate to severe pain in adults.
The extended-release-tablet formulation of this drug is used to treat moderate to severe chronic pain when treatment is needed around the clock.
This medication must be prescribed by a doctor and is available by prescription only.
Patients taking this drug should alert their doctors about any problems from the use of this medication and any unusual side effects or symptoms or troublesome side effects.
Care should be taken to ensure this medication is taken exactly as prescribed.
The risk of addiction to most opioid medications is usually, high. However, the risk of addiction to Tramadol is not high.
Read the patient health information leaflet that accompanies the prescription of this medication as well as every time the prescription is refilled. There may be new health care information.
WHAT ARE THE DOSAGES?
Dosages of Tramadol Should Be Given As Follows:
- Tincture: 5-15 drops or 1-3 drops of fluid extract.
Adult Dosage Forms & Strengths
Tablet: Schedule IV
- 10 mg/mL
Capsule, Extended Release: Schedule IV
- 100 mg (ConZip, Ultram ER)
- 150 mg (ConZip)
- 200 mg (ConZip, Ultram ER)
- 300 mg (ConZip, Ultram ER)
Pediatric Dosing Forms & Strengths:
Tablet: Schedule IV
- Oral dose 50 mg
- 10 mg/mL
Extended-release capsule or oral tablet must not be chewed, crushed, split, or dissolved. Also combined with acetaminophen.
- Chronic: 25 mg oral dose every morning initially; increase by 25-50 mg/day every 3 days up to 50-100 mg orally every 4-6hr as needed; not to exceed 400 mg/day
- Acute: 50-100 mg oral dose every 4-6hr as needed; not to exceed 400 mg/day
- 100 mg orally once daily initially; increase by 100 mg/day every 5 days; not to exceed 300 mg/day
- Conversion from immediate release to extended release: Round total daily dose down to nearest 100 mg
- Do not chew, crush, split, or dissolve
- Severe renal impairment (CrCl less than 30 mL/min): Immediate release, 50-100 mg orally every 12hr; extended-release not recommended
- Severe hepatic impairment: Immediate release, 50 mg oral tablets every 12hr; extended-release not recommended
Pediatric Dosage Considerations
- Treatment for patients under 17 years: Safety and efficacy not established
- Treatment for patients 17 years and older (acute): 50-100 mg oral tablets every 4-6hr as needed; not to exceed 400 mg/day
- Treatment for patients 17 years and older (chronic): 25 mg oral tablets every morning initially; increase by 25-50 mg/day every 3 days as separate doses up to 50-100 mg orally every 4-6hr as needed; not to exceed 400 mg/day
- Treatment for under 18 years: Safety and efficacy not established. May cause risks to health.
Geriatric Dosage Forms and Strengths:
- Treatment for under 65 years: Initiate at the lower end of dosing range; not to exceed 300 mg/day if over 75 years.
- Treatment for under 75 years: Not to exceed 300 mg of medicine per day; immediate release; use great caution with the extended-release formulation of this medicine
- Side Effects
- Drug Interactions
- Warnings and Precautions
WHAT ARE SIDE EFFECTS ASSOCIATED WITH USING TRAMADOL (ULTRAM)?
Side effects associated with use of Tramadol, include the following:
WHAT ARE WARNINGS AND PRECAUTIONS FOR TRAMADOL (ULTRAM)?
This medication contains tramadol. Do not take Ultram, Ultram ER, Ryzolt or ConZip if you are allergic to tramadol or any ingredients contained in this drug.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center immediately.
Contraindications include hypersensitivity to tramadol or opioids. Known or suspected gastrointestinal obstruction, including paralytic ileus. Concurrent use of monoamine oxidase inhibitors (MAOIs) or use within last 14 days.
Effects of Drug Abuse
Risk of potentiating opioid addiction, abuse, and misuse, which can lead to overdose and death; assess each patient’s risk prior to prescribing and monitor all patients regularly for the development of these behaviors or conditions.
Pregnancy and Lactation
Pregnancy: Prolonged use of opioid analgesics during pregnancy for medical or nonmedical purposes can result in physical dependence in the neonate and neonatal opioid withdrawal syndrome shortly after birth.
- Medical professionals should observe newborns for symptoms of neonatal opioid withdrawal syndrome and manage accordingly.
- Neonatal seizures, neonatal withdrawal syndrome, fetal death, and stillbirth have been reported with tramadol during post-approval use of tramadol immediate-release products.
Lactation: Monitor infants exposed through breast milk for excess sedation, respiratory depression, or other health problems; withdrawal symptoms can occur in breastfed infants when maternal administration of an opioid analgesic is stopped, or when breastfeeding is stopped.
Talk with your doctor if you have any questions about pregnancy and breastfeeding while taking this medicine.