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Avdol (Tramadol)

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Avdol is a narcotic-like pain relieving oral medicine that is used as a treatment for moderate to severe pain in adults. This medication must be prescribed by a doctor and is available by prescription only.

Other names for this medication:
Acupain, Acuvin, Adamon, Admadol, Anatram, Antram, Arrestadol, Damadol, Damol, Domaspas, Ivydol, Mandol, Muzox, Nomadol, Novadol, Ondol, Opiran, Radol, Redimol, Sayodol, Sedate, Supridol, Takol, Tramagesic, Tramak, Tramed, Tramest, Tramoflex, Tramot, Tranat, Trandol, Transic, Tridol, Trydol, Typhon, Vardol

Similar Products:
Viagra, Symmetrel, Amethopterin, Diflucan, Ambien, Thorazine, Requip, Hytrin, Deltasone, Danocrine

Also known as: Tramadol


{name} (tramadol) is a pain medicine similar to an opioid. It acts in the central nervous system (CNS) to relieve pain.

{name} is used to treat moderate to severe pain in adults.

The extended-release form of tramadol ({name} ER) is for around-the-clock treatment of pain. {name} ER is not for use on an as-needed basis for pain.


Usual Adult Dose for Pain:

Adults (17 years or older): 50 to 100 mg orally every 4 to 6 hours as needed for pain -For patients not requiring rapid onset of analgesic effect: Initial dose: 25 mg orally once a day; titrate in 25 mg increments every 3 days to reach a dose of 25 mg four times a day; thereafter increase by 50 mg as tolerated every 3 days Maximum dose: 400 mg per day.

Usual Adult Dose for Chronic Pain:

Extended-Release (ER): 18 years or older (tramadol-naive): 100 mg orally once a day -Individually titrate in 100 mg increments every 5 days to an effective dose that minimizes adverse reactions -Maximum Dose: 300 mg/day For patients CURRENTLY receiving Immediate-Release (IR) Avdol: Initial Dose: Calculate 24-hour IR requirement and initiate with a total daily ER dose rounded down to the next lowest 100 mg increment orally once a day Conversion from OTHER Opioids: Discontinue all other around the clock opioid drugs prior to initiating therapy -Initial dose: 100 mg ER orally once a day -Individually titrate in 100 mg increments every 5 days to an effective dose that minimizes adverse reactions -Maximum Dose: 300 mg/day.

Usual Geriatric Dose for Pain:

Dose selection should be cautious generally starting at the low end of the dose range Over 75 years: Maximum dose of Immediate-release: 300 mg per day.

Usual Geriatric Dose for Chronic Pain:

Dose selection should be cautious generally starting at the low end of the dose range Over 75 years: Maximum dose of Immediate-release: 300 mg per day.

Usual Pediatric Dose for Pain:

Avdol is not recommended for use in pediatric patients 17 years or older: See Adult Dose.

Detailed Avdol dosage information


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. An overdose can be fatal, especially in a child or other person using the medicine without a prescription. Overdose symptoms may include severe drowsiness, pinpoint pupils, slow breathing, or no breathing.

Your doctor may recommend you get naloxone (a medicine to reverse an opioid overdose) and keep it with you at all times. A person caring for you can give the naloxone if you stop breathing or don't wake up. Your caregiver must still get emergency medical help and may need to perform CPR (cardiopulmonary resuscitation) on you while waiting for help to arrive.

Anyone can buy naloxone from a pharmacy or local health department. Make sure any person caring for you knows where you keep naloxone and how to use it.


Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture and heat. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Avdol are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.


You should not take Avdol ER if you are allergic to it, or if you have:

severe asthma or breathing problems; a stomach or bowel obstruction (including paralytic ileus); if you have recently used alcohol, sedatives, tranquilizers, or narcotic medications; or if you have used an MAO inhibitor in the past 14 days (such as isocarboxazid, linezolid, methylene blue injection, phenelzine, or tranylcypromine).

Avdol ER should not be given to a child younger than 12 years old. Avdol ER should not be given to anyone younger than 18 years old.

Do not give Avdol ER to anyone younger than 18 years old who recently had surgery to remove the tonsils or adenoids.

Seizures have occurred in some people taking Avdol ER. Your seizure risk may be higher if you have ever had:

a head injury, epilepsy or other seizure disorder; drug or alcohol addiction; or a metabolic disorder.

Tell your doctor if you have ever had:

breathing problems, sleep apnea; liver or kidney disease; urination problems; problems with your gallbladder, pancreas, or thyroid; a stomach disorder; or mental illness, or suicide attempt.

If you use Avdol ER during pregnancy, your baby could be born with life-threatening withdrawal symptoms, and may need medical treatment for several weeks.

Ask a doctor before using Avdol ER if you are breastfeeding. Tell your doctor if you notice severe drowsiness or slow breathing in the nursing baby.

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Division of the chloroplast envelope membrane is performed by constriction of the ring structures at the division site. The reaction of iodine with preparations of the thyreotrophic hormone. Here, we silenced the taxol-sensitizer genes identified (acrbp, atp6v0d2, fgd4, hs6st2, psma6, and tubgcp2) in nine other cancer cell types (including lung, cervical, ovarian, and hepatocellular carcinoma cell lines) that showed reduced cell viability in the presence of a sub-lethal concentration of taxol. Attentional retraining procedures: manipulating early or late components of attentional bias?. Serum samples from 9 of 10 bleeding occasions were tested using an epitope-blocking enzyme-linked immunosorbent assay for the presence of antibodies to influenza A virus. Relationship between the fimA genotype and pathogenicity of Porphyromonas gingivalis. Abnormal inflammatory activity returns after natalizumab cessation in multiple sclerosis. These results demonstrate that NCQ-344 is capable of facile formation of a reactive para-quinone capable of reacting with GSH and may rationalize previous findings regarding the biological effects observed in vitro with these two remoxipride metabolites.

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A global spatial statistic was used to detect area-wide trends of clustering for human infection at the household level. The role of MCP-1 may be to recruit mononuclear cells (monocytes) to the dental follicle, where these cells, in turn, fuse to form osteoclasts to resorb alveolar bone for the formation of an eruption pathway. peronaeus longus in the treatment of paralytic talipes calcaneus. Moisture transfer into medicament chambers equipped with a double-barrier-desiccant system. MMN/NP3 amplitudes and latencies were compared between groups and were correlated with trait (PSYRATS) and state measures of AH severity as well as clinical symptom ratings in SZs.SZ patients (vs.

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Multi-detector row CT: effect of iodine dose reduction on hepatic and vascular enhancement. Nevertheless, liver tumors and cultured hepatoma cell lines proliferate in the presence of C/EBPalpha. An explanation for the absence of effect of Infliximab on insulin resistance in morbidly obese subjects may be the paracrine way of action of this cytokine. Measurements of the facial recess anatomy: implications for sparing the facial nerve and chorda tympani during posterior tympanotomy. There is increasing interest in the use of combination therapy for rheumatoid arthritis and in the possibility of combining the conventional drug approach with newer biological therapies.

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Hydrodynamic mobility of an optically trapped colloidal particle near fluid-fluid interfaces. To address the role of this gene in inner ear development, we blocked BMP4 function(s) by delivering one of its antagonists, Noggin, to the developing inner ear in ovo. Decrease in endothelial nitric oxide synthase (eNOS) expression is one of the adverse outcomes of endothelial dysfunction. Topsoil (0-5 cm) composition in eight arctic catchments in northern Europe (Finland, Norway and Russia). Analysis of Tyr to Phe and fa/fa leptin receptor mutations in the PC12 cell line. Reduction of Fusarium head blight and deoxynivalenol in wheat with early fungicide applications of prothioconazole. The defibrillation threshold (DFT) of a transvenous-subcutaneous electrode configuration is sometimes unacceptably high. This sign is commonly deemed to signify on ominous pathology and suggests the presence of pancreatic or biliary malignancy. Cells lacking different myosin I pairs (myoA-/myoB-, myoB-/myoC-, and myoA-/myoC-) were examined with respect to their cytoskeletal organization.

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Effects of neurotensin administered into the ventral tegmental area on prepulse inhibition of startle. Recognizing independent and joint activities among multiple residents in smart environments. Retrospective analysis of registry database of the National Hospital Study Group for Lung Cancer (NHSGLC) between 1990 and 2005. Enhanced rate of degradation of basic proteins by 26S immunoproteasomes. The neurological optimality score of 21 full term healthy, neurologically normal newborn infants was determined by two well trained observers. The technology also facilitates surface reconstruction, in which facial features and, as a result, patient identity may be recognized, leading to risk of violations of patient privacy rights. Under nondenaturing, but reducing, conditions the in vitro-translated 54K polypeptide forms oligomers (probably tetramers) of molecular weight approximately 2 x 10(5). A filter design methodology based on a simple batch test and numerical simulations is proposed. Development of a frequency-separated knob with variable change rates by rotation speed.

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