Suppositories route

The suppositories route is used to administer medication through the rectum or vagina. The rectum contains many capillaries that increase the absorption of the medication. Rectal suppositories are used when ... 

The suppository route is used to administer medication through the rectum and the vagina. A route that few patients look forward to is the parenteral route because medication is given using injections or directly into the vein, the intravenous (IV) routes. 

The suppository route is used to absorb medication directly into the rectum or vagina. The parenteral route is used to inject medication directly into the dermal or subcutaneous tissue, muscle, or into the veins. 

If theophylline or anotiier xanthine derivative is given as a rectal suppository, the nurse checks die patient every 15 to 30 minutes to be sure die suppository has been retained. If the patient is unable to retain die suppository, die nurse contacts the primary health care provider because anodier route of administration may be necessary. 

Use the oral route of administration if the patient has mild nausea with minimal or no vomiting. Seek an alternative route (e.g., transdermal, rectal suppository, or parenteral) if the patient is unable to retain oral medications due to vomiting. 

Diazepam Being extremely lipophilic, diazepam penetrates quickly into the CNS, but can rapidly redistribute into body fat and muscle. This results in a faster decline in CNS levels and early recurrence of seizures. It is dosed at 5 to 10 mg (or 0.15 mg/kg) and infused no faster than 5 mg/minute. Repeated doses can be given every 5 minutes until seizure activity stops or toxicities are seen (e.g., respiratory depression). Diazepam can also be administered as a rectal suppository, making it possible for non-medical personnel to provide rapid therapy for seizures that develop at home or in public areas.11 The adult dose is 10 mg given rectally and this dose may be repeated once if necessary. Diazepam is erratically absorbed via the intramuscular route therefore, IM administration is not recommended. 

Rectal Administration. The administration of drugs by a solid rectal dosage form (i.e., suppositories) results in a wide variability in the rate and extent of absorption in children [79]. This fact, coupled with the inflexibility of a fixed dose, makes this a route that should not be promoted for pediatric patients. At least one death involving a 7-month-old infant can be directly attributed to the use of solid rectal dosage form of a therapeutic dose of morphine [80]. 

For routes of administration in which the chemical is given orally or placed into an orifice other than the mouth, clear instructions about the correct administration of the chemical must be provided. Many cases are known of oral pediatric drops for ear infections being placed into the ear, and vice versa (ear drops being swallowed) in humans. Errors in test-article administration are especially prevalent when a chemical form is being used in a nontraditional manner (e.g., suppositories that are given by the buccal route). 

Diclofenac is available as dispersible tablets, tablets, gel, suppositories and for intravenous or intramuscular injection. The maximum dose of diclofenac administered via any route is 150 mg. As v/ith other non-steroidal anti-inflammatory drugs, concomitant use in patients receiving venlafaxine increases the risk of bleeding. 

Diphenolmethane derivatives (p. 177) were developed from phenolphthalein, an accidentally discovered laxative, use of which had been noted to result in rare but severe allergic reactions. Bisac-odyl and sodium picosulfate are converted by gut bacteria into the active colon-irritant principle. Given by the enteral route, bisacodyl is subject to hydrolysis of acetyl residues, absorption, conjugation in liver to glucuronic acid (or also to sulfate, p. 38), and biliary secretion into the duodenum. Oral administration is followed after approx. 6 to 8 h by discharge of soft formed stooL When given by suppository, bisacodyl produces its effect within 1 h. 

Absorption - Theophy ne is well absorbed from oral liquids and uncoated plain tablets maximal plasma concentrations are reached in 2 hours. Rectal absorption from suppositories is slow and erratic, the oral route is generally preferred. Enteric-coated tablets and some sustained-release dosage forms may be unreliably absorbed. 

Drugs are administrated by intravenous routes or ex-travascular routes including oral, sublingual, subcutaneous, intramuscular, rectal (by enema or suppository), and transdermal. Available dosage forms include suspensions, immediate-release capsules or tablets, sustained-release capsules or tablets, and enteric-coated capsules or tablets that resist dissolution in the acidic pfi of the stomach. 

The hepatic first-pass effect can be avoided to a great extent by use of sublingual tablets and transdermal preparations and to a lesser extent by use of rectal suppositories. Sublingual absorption provides direct access to systemic—not portal—veins. The transdermal route offers the same advantage. Drugs absorbed from suppositories in the lower rectum enter vessels that drain into the inferior vena cava, thus bypassing the liver. However, suppositories tend to move upward in the rectum into a region where veins that lead to the liver predominate. Thus, only about 50% of a rectal dose can be assumed to bypass the liver. 

Suppositories are pharmaceutical dosage forms intended for administration of medicine via the rectum, vagina, or urethra that melt, soften, or dissolve in the body cavity. Rectal and vaginal suppositories are most common but urethral suppositories are sometimes used. Suppositories are indicated for administering drugs to infants and small children, severely debilitated patients, those who cannot take medications orally, and those for whom the parenteral route might be unsuitable. Suppositories are used to administer drugs for either systemic or local application. Local applications include the... 

Dosages and routes of administration Morphine is available in different salt forms but the hydrochloride and sulfate (Vermeire and Remon, 1999) are used preferentially. The compound can be administered by the oral, parenteral or intraspinal route. Oral application is preferred for chronic pain treatment and various slow release forms have been developed to reduce the administration frequency to 2-3 times per day (Bourke et al., 2000). Parenteral morphine is used in intravenous or intramuscular doses of 10 mg, mostly for postoperative pain and self-administration devices are available for patient-controlled analgesia (PCA). Morphine is additionally used for intraspinal (epidural or intrathecal) administration. Morphine is absorbed reasonably well in the lower gastrointestinal tract and can be given as suppositories. 

Dosages and routes of administration Oxymorphone is used parenterally by intramuscular or subcutaneous doses of 1-1.5 mg and as suppositories with a content of 5 mg. For patient controlled analgesia (PCA) i.v. bolus doses up to 300 pg are used (Sinatra and Harrison, 1989). 

Orifices. Include eye, ear, nose, throat, rectal, vaginal, and the mouth as a route to the throat and lungs, orifices using suppositories, pessaries, drops, solutions, ointments, gases, vapors, aerosols, and inhalations. 

The rectal milieu is quite constant as its pH is about 7.5, and the temperature is usually 37°C. It is normally empty and the pressure varies between 0 and 50 cm. This makes this route suitable for the (controlled) delivery of drugs by applying adequate (controlled release) dosage forms such as osmotic pumps and hydrogels, since the classical suppositories are, in general, not the most suitable dosage form to achieve a reproducible rate and extent of drug absorption. 

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