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Cadol (Tramadol)
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Cadol

Cadol 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, Anazac, Cadol, Cemadol, Cosdol, Cradol, Doleira, Dolfre, Dolmeri, Domaspas, Euphodol, Formador, Lagesic, Medol, Mobiya, Omodol, Opidol, Orchidol, Pacadon, Postadol, Sedate, Supridol, Taramol, Tramadol, Tramaflam, Tramared, Tramataur, Trambax, Tramed, Tramest, Tramex, Tranat, Tranzat, Trapain, Trasic, Vardol

Similar Products:
Benemid, Eldepryl, Zanaflex, Leukeran, Atarax, Crestor, Minocin

Also known as: Tramadol

Description

{name} ER is an pain medicine similar to an opioid. This medicine is used to treat moderate to severe pain.

The extended-release form of tramadol is for around-the-clock treatment of pain. This form of tramadol is not for use on an as-needed basis for pain.

Dosage

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) Cadol: 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:

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

Detailed Cadol dosage information

Overdose

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.

Storage

Store at room temperature between 15 and 25 degrees C (59 and 77 degrees F) away from moisture, light and heat. Keep container tightly closed. Keep out of the reach of children.

Side effects

The most common side effects associated with Cadol 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.

Contraindications

Do not drink alcohol. Dangerous side effects or death could occur.

Avoid driving or hazardous activity until you know how this medicine will affect you. Dizziness or drowsiness can cause falls, accidents, or severe injuries.

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Acute respiratory distress syndrome (ARDS) is the most severe form of lung injury, characterised by alveolar oedema and vascular permeability, in part due to disruption of the alveolar capillary membrane integrity. HERC2-USP20 axis regulates DNA damage checkpoint through Claspin. However, the role of additives in xylan hydrolysis by xylanase is not yet clear. Comparative evaluation of chromogenic agar medium and conventional culture system for isolation and presumptive identification of uropathogens. To determine the extent to which prostheses with no readily available evidence to support their use are being implanted in primary total hip arthroplasty. Radiographs revealed typical bilateral, symmetric osteosclerosis of the metaphyseal regions of long bones of the upper and lower extremities.

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Pooled estimates were computed for subgroups of studies with similar patients in similar settings. This article discusses the efficacy, safety, and tolerability of ketamine, summarizes the neurobiology of depression, reviews the mechanisms underlying the rapid antidepressant effects of ketamine, and discusses the prospects for next-generation rapid-acting antidepressants. In response to large, bright stimuli that activate their surrounds, rods depolarize. Repeated provocation of time- and ATP-induced early pulmonary vein reconnections after pulmonary vein isolation: eliminating paroxysmal atrial fibrillation in a single procedure. Individual lifespans of isogenic organisms, such as Caenorhabditis elegans nematodes, fruit flies, and mice, vary greatly even under identical environmental conditions. We prefer the nonlinear approach, as we believe that the effects are taking place in a subtle way, since there is no direct correlation between reflexological points and modern neuroanatomy. Production and characterization of a monoclonal antibody to partially purified estrogen receptor from human breast tumor. The purpose of this systematic review was to identify, with supporting evidence, the effect of infertility on couples. Sensory hair fusion and glycocalyx changes after gentamicin exposure theolair 250 mg in the guinea pig.

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Experience with the study and organization of the teaching of hygiene to students in the lower grades. The capactins, a class of proteins that cap the ends of actin filaments. The new perforated PDS foil turned out to be easier to handle intraoperatively because of smooth and clean cutting edges. Infliximab 5 mg/kg was given at week 0, 2, 6, and every 8 weeks thereafter. Although there has been an exponential rise in the volume of research generated about it for both medical and surgical uses, key questions remain about its actual benefits. This, coupled with results obtained from experiments examining the time course of synapse formation, led us to propose that the extent to which LA-N-2 cells in our coculture system are differentiated may vary and that this variation may underlie the degree to which they express neuron-like transmission properties. Very preterm infants exhibit reduced thalamocortical connectivity and cortical neuroplasticity compared with term-born controls. This effect was time and dose dependent, and the effective dose ranging from (20-200 U/ml). Nanochannel-based electrochemical assay for transglutaminase activity.

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Cyanate triggers ICAM-1 expression through a mechanism depending on activation of the mitogen-activated protein kinase p38 and nuclear factor-kappaB. Thus, the facilitation of self-stimulation by chlordiazepoxide, pentobarbitone and clonazepam appears to be accounted for in terms of non-gabergic anti-conflict activity by these agents. Such knowledge will be critical for drug design against the NHERF1 PDZ1 domain, highlighting the continued need for experimentally determined PDZ1-ligand complexes. Keeping children active is an important goal to ensure healthy physical and social development. Meanwhile, correlation between RXP and bioactivity,components was investigated. To determine nutritional intake and vitamin status in a sample of homeless people who had been on the streets of Paris for more than 2 y. The Doi-Edwards theory is found to be applicable but only by taking into account the shear-rate-dependence of the terminal relaxation time.

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