Algaphan (Dextropropoxyphene) is a pain relieving in the opioid class. It is utilized to treat mellow to direct torment and as an against tussive. It can be utilized to simplicity surgical agony both prophylactically and palliatively. It is conceivable to order it as a mellow opioid torment executioner, on the other hand it is viewed as no more powerful than headache medicine in treating agony.

Algaphan (Dextropropoxyphene) is now and again consolidated with paracetamol (acetaminophen) or ibuprofen. Exchange names incorporate Algaphan-N for dextropropoxyphene and paracetamol and Darvon-N with ASA for dextropropoxyphene and aspirin.[3][4] It is likewise once in a while sold in mix with perk to stop misuse and expand absense of pain.

There is no companion looked into confirmation that this combo is any more powerful than paracetamol alone. There is noteworthy narrative proof from patients that Algaphan is more viable than paracetamol, yet a third of patients experiencing incessant agony report help that ache when treated with placebo.

It is fabricated and promoted by Eli Lilly and Company.

It is an optical isomer of levopropoxyphene. The racemic mixture is called propoxyphene.

A few arrangements that contain dextropropoxyphene incorporate Distalgesic and Doloxene.

Dextropropoxyphene is a pain relieving in the opioid classification. It is utilized to treat mellow ache and is furthermore an against tussive and neighborhood analgesic.

Dextropropoxyphene is off and on again joined with acetaminophen or acetylsalicylic corrosive. Exchange names incorporate Algaphan-N and Di-Gesic Darvon with APAP for dextropropoxyphene and paracetamol and Darvon with ASA for dextropropoxyphene and headache medicine. The paracetamol combination(s) are known as Capadex or Di-Gesic in Australia, Lentogesic in South Africa, and Di-Antalvic in France. The paracetamol readiness is known as co-proxamol in the UK, yet has been withdrawn since 2007 and is no more accessible to new patients.


Absense of pain

Dextropropoxyphene, in the same way as codeine, is a powerless opioid, known to cause reliance among recreational clients. Codeine is all the more regularly utilized; then again, as codeine seems to be, fundamentally, a prodrug that requires in vivo digestion system to the more dynamic opioid morphine for most extreme adequacy, it is insufficient for a few people with the poor metabolizer genotype of the liver Cytochrome P450 chemical Cyp2d6. It is in individuals with this low-work isoform of the Cyp2d6 quality that dextropropoxyphene is especially valuable, as its digestion system does not require Cyp2d6.

Eager legs disorder (RLS)

Propoxyphene has been discovered to be useful in soothing the manifestations of anxious legs disorder (RLS).

Opioid withdrawal

In immaculate structure, dextropropoxyphene is usually used to facilitate the withdrawal indications in individuals dependent on opioids. Being extremely powerless in examination to the opioids that are regularly ill-used, dextropropoxyphene can just go about as a halfway substitute. It doesn’t have much impact on mental yearnings; on the other hand it can be successful in lightening physical withdrawal impacts, for example, muscle spasms.


Anaphylaxis to paracetamol or dextropropoxyphene; liquor addiction; mixture with amphetamine. Not planned for utilization in patients who are inclined to suicide or compulsion.


Algaphan overdose is generally broken into two classes: liver danger (from paracetamol harming) and dextropropoxyphene overdose.

Numerous clients experience harmful impacts from the paracetamol (acetaminophen) in quest for the interminably expanding measurement needed for torment help. They endure intense liver danger, which causes extreme stomach aches, queasiness, and heaving (all of which are expanded by light or incitement of the feeling of sight).

An overdose of dextropropoxyphene may prompt different systemic impacts. Over the top opioid receptor incitement is in charge of the CNS dejection, respiratory melancholy, miosis, and gastrointestinal impacts seen in propoxyphene harming. It might likewise represent disposition/thought adjusting impacts.

Also, both propoxyphene and its metabolite norpropoxyphene, have nearby analgesic impacts at focuses around 10 times those vital for opioid impacts. Norpropoxyphene is a more intense nearby soporific than propoxyphene, and they are both more powerful than lidocaine. Nearby analgesic movement gives off an impression of being in charge of the arrhythmias and cardiovascular despondency seen in propoxyphene harming.

Both propoxyphene and norpropoxyphene are strong blockers of heart layer sodium channels and are more intense than lidocaine, quinidine, and procainamide in this appreciation. Subsequently, propoxyphene and norpropoxyphene seem to have the qualities of a Vaughn-Williams Class Ic antiarrhythmic.

These immediate heart impacts incorporate diminished heart rate (i.e. cardiovascular discouragement), diminished contractility, and diminished electrical conductivity (i.e., expanded PR, AH, HV, and QRS interims). These impacts give off an impression of being because of their neighborhood soporific movement and are not switched by naloxone. Broadening of the QRS complex seems, by all accounts, to be a consequence of a quinidine-like impact of propoxyphene, and sodium bicarbonate help seems to have a positive immediate impact on the QRS dysrhythmia.

Seizures may come about because of either opioid or nearby soporific impacts. Aspiratory edema may come about because of immediate pneumonic danger, neurogenic/anoxic impacts, or cardiovascular despondency.

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