Tramadol Pill 50mgIT
Tramadol Pill 50mg to Treat moderate pain
Tramadol is a prescription opioid drug intended to treat moderate to severe pain. However, like other narcotic medicines, it comes with a potential for addiction. It takes a considerate amount of time as well as effort to get addicted to it. Tramadol Pill 50mg for relief from pain while staying at home.
In addition to this, each pill also contains the below mentioned inactive ingredients:
- Magnesium stearate
- Croscarmellose sodium
- Lactose monohydrate
- Microcrystalline cellulose
- Polyethylene glycol
- Titanium dioxide
- Pregelatinized starch
The mode of action of Tramadol pills works on two mechanisms:
- Weak inhibition of reuptake of serotonin and norepinephrine
- Binding of parent and M1 metabolite to opioid receptors
This drug is seen to inhibit the reuptake of neurotransmitters, namely serotonin and norepinephrine in vitro as is the case with some other opioid pain drugs. These mechanisms may independently contribute to the analgesic profile of tramadol hydrochloride. In human beings, analgesic may begin within an hour of ingesting the dose and can hit the peak in around two to three hours.
Other than analgesia, administration of tramadol hydrochloride may produce a host of symptoms similar to the ones produced by other opioid drugs such as the following:
Tramadol, in contrast to morphine, has not shown to cause release of histamine. If this drug is taken in therapeutic dosage amounts, it will not have any adverse effect on the following body functions:
- Left-ventricular function
- Heart rate
- Cardiac index
Though, orthostatic hypotension is observed.
When you take tramadol hydrochloride orally with food, it does not have any significant effect on its rate or extent of absorption. Hence, you may take this medicine either with food or without food.
Metabolism of Tramadol tablets
Tramadol pain pills are extensively broken down after it is ingested orally. Around thirty percent of the dose amount is excreted by way of urine as unchanged medicine while the sixty percent of the dose amount is excreted as metabolites. The remaining ten percent is either excreted as unextractable or unidentified metabolites. The most important metabolic pathways seem to be N- and O-demthylation and glucoronidation or sulfation in the liver. Formation of M1 metabolite depends on CYP2D6 and hence, is subject to inhibition that may have an effect on the therapeutic response.
Around seven percent of the population has decreased activity of the CYP2D6 isoenzyme of cytochrome P-450. These people are “poor metabolizers” of the following medicines, among other drugs:
- Tricyclic antidepressants
Purchase Tramadol online for effective management of pain. It has been seen that the concomitant usage of MAO inhibitors and serotonin reuptake inhibitors may heighten the risk of you experiencing adverse effects that may include the following:
- Serotonin syndrome