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2. Macrogol - Wikipedia

   en.wikipedia.org/wiki/Macrogol

   Macrogol 4000, pharmaceutical quality. Macrogol 3350, often in combination with electrolytes, is used for short-term relief of constipation as well as for long-term use in constipation of various causes, including in multiple sclerosis and Parkinson's disease patients (an often-overlooked non-motor symptom) as well as constipation caused by pharmaceutical drugs such as opioids and ...

3. First pass effect - Wikipedia

   en.wikipedia.org/wiki/First_pass_effect

   [1] [2] The effect is most associated with orally administered medications, but some drugs still undergo first-pass metabolism even when delivered via an alternate route (e.g., IV, IM, etc.). [3] During this metabolism, drug is lost during the process of absorption which is generally related to the liver and gut wall. The liver is the major ...

4. Laxative - Wikipedia

   en.wikipedia.org/wiki/Laxative

   Prolonged use of stimulant laxatives can create drug dependence by damaging the colon's haustral folds, making users less able to move feces through their colon on their own. A study of patients with chronic constipation found that 28% of chronic stimulant laxative users lost haustral folds over the course of one year, while none of the control ...

5. Drug antagonism - Wikipedia

   en.wikipedia.org/wiki/Drug_antagonism

   Drug antagonism refers to a medicine stopping the action or effect of another substance, preventing a biological response. [1] [2] The stopping actions are carried out by four major mechanisms, namely chemical, pharmacokinetic, receptor and physiological antagonism. [2] The four mechanisms are widely used in reducing overstimulated ...

6. Prostaglandin inhibitors - Wikipedia

   en.wikipedia.org/wiki/Prostaglandin_inhibitors

   Prostaglandin inhibitors are drugs that inhibit the synthesis of prostaglandin in human body. [1] There are various types of prostaglandins responsible for different physiological reactions such as maintaining the blood flow in stomach and kidney, regulating the contraction of involuntary muscles and blood vessels, and act as a mediator of inflammation and pain.

7. Drug permeability - Wikipedia

   en.wikipedia.org/wiki/Drug_permeability

   Equation 1: = / / The drug apparent permeability (P app) is calculated by normalizing the drug flux (j) over the initial concentration of the API in the donor compartment (c 0) as: Equation 2: = / Dimensionally, the P app represents a velocity, and it is normally expressed in cm/sec. The highest is the permeability, the highest is expected to ...

8. Absorption (pharmacology) - Wikipedia

   en.wikipedia.org/wiki/Absorption_(pharmacology)

   Absorption is the journey of a drug travelling from the site of administration to the site of action. [ 1 ] [ 2 ] The drug travels by some route of administration ( oral , topical-dermal , etc.) in a chosen dosage form (e.g., tablets , capsules , or in solution ). [ 3 ]

9. Mechanism of action of aspirin - Wikipedia

   en.wikipedia.org/wiki/Mechanism_of_action_of_aspirin

   Newer NSAID drugs called COX-2 selective inhibitors have been developed that inhibit only COX-2, with the hope for reduction of gastrointestinal side-effects. [8] However, several COX-2 selective inhibitors have subsequently been withdrawn after evidence emerged that COX-2 inhibitors increase the risk of heart attack. [ 9 ]