Related Searches : BENZPHETAMINE HCL 50 MG TABLETmeperidine 100mgdemerolEphedrine HCL 30mgpseudoephedrine hcl 60mg tabletsPhentermine 37.50mg

Demerol (meperidine hcl) 50 mg

  • USD 1 - 2 / Piece  [Get Latest Price]
  • 1000 Piece/Pieces
  • Other
  • Meperidine hcl
  • 50mg
  • Tablets
  • Demerol (meperidine hcl) 50 mg
  • Supplier - Pills Medicine Store Ltd
  • GeorgiaGeorgia
  • 51 - 100 People
  • Manufacturer,Distributor/Wholesaler,Agent
  • North America,South America,Eastern Europe,Southeast Asia,Africa,Oceania,Mid East,Eastern Asia,Western Europe
  • Mr.Durell
  • 995-32-717274
Post Date : July 27
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Meperidine hcl


Meperidine hydrochloride is ethyl 1-methyl-4-phenylisonipecotate hydrochloride, a white crystalline substance with a melting point of 186°C to 189°C. It is readily soluble in water and has a neutral reaction and a slightly bitter taste. The solution is not decomposed by a short period of boiling.

Each tablet for oral administration contains 50 mg or 100 mg of meperidine hydrochloride. They are white, unscored, round, biconvex tablets. In addition, each tablet contains the following inactive ingredients: confectioners sugar, lactose monohydrate, magnesium stearate, povidone and sodium starch glycolate.

Meperidine hydrochloride is a narcotic analgesic with multiple actions qualitatively similar to those of morphine; the most prominent of these involve the central nervous system and organs composed of smooth muscle. The principal actions of therapeutic value are analgesia and sedation.

There is some evidence which suggests that meperidine may produce less smooth muscle spasm, constipation, and depression of the cough reflex than equianalgesic doses of morphine. Meperidine, in 60 mg to 80 mg parenteral doses, is approximately equivalent in analgesic effect to 10 mg of morphine. The onset of action is slightly more rapid than with morphine, and the duration of action is slightly shorter. Meperidine is significantly less effective by the oral than by the parenteral route, but the exact ratio of oral to parenteral effectiveness is unknown.

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Using clonazePAM together with temazepam may increase side effects such as dizziness, drowsiness, and difficulty concentrating. Some people may also experience some impairment in thinking and judgment. You should avoid or limit the use of alcohol while being treated with these medications. Avoid driving or operating hazardous machinery until you know how the medications affect you. It is important to tell your doctor about all other medications you use, including vitamins and herbs. Do not stop using any medications without first talking to your doctor.

Clonazepam (1 mg h.s.) and temazepam (30 mg h.s.) were studied in 10 patients diagnosed as having insomnia with nocturnal myoclonus. Each subject underwent two nocturnal polysomnographic recordings while drug-free, two during treatment with clonazepam, and two during treatment with temazepam. Treatment sessions were 7 days long, and recordings were done on nights 6 and 7 of the treatment sessions. A 14-day washout period separated the treatment sessions. The order of drugs used in the first and second treatment sessions was randomized. Objective and subjective sleep laboratory data showed that both drugs improved the sleep of patients with insomnia in association with nocturnal myoclonus. Neither drug significantly reduced the number of nocturnal myoclonic events. Sleep changes were consistent with those produced by sedative benzodiazepines in general. Thus, the data support clinical reports that clonazepam, a benzodiazepine marketed for the indication of seizure, is useful in improving sleep disturbances associated with nocturnal myoclonus. Temazepam, a benzodiazepine marketed for the indication of insomnia, was found to be a suitable alternative to clonazepam in the treatment of insomnia associated with nocturnal myoclonus. The present data and other studies suggest the need for a model that explains why leg movements and sleep disturbances may wax and wane independently.

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fentynol 5ml/.005mg

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Fentanyl Citrate Injection (CII) 0.05mg/ml, 5ml vial, 25 vials/pack

Fentanyl is available as a skin patch, lozenge, pills, shots, a film that dissolves in your mouth, or by IV (intravenous).

Use fentanyl exactly as prescribed by your doctor. This is very important so that you do not get too much of the drug. If you get too much fentanyl in your system, you could have serious problems that can lead to death.

How It Works

Fentanyl acts upon specific receptors in your brain and spinal cord to decrease the feeling of pain and to reduce your emotional response to pain. The action of fentanyl is similar to other drugs in the morphine category (opioids).

Why It Is Used

Fentanyl is used to manage moderate to severe pain, usually in people who have chronic pain. Fentanyl is often used when your other pain medicines no longer work.

How Well It Works

For people with cancer who are already on opioid pain medicine such as morphine or oxycodone, fentanyl works well for treatment of cancer pain.1

Side Effects

Fentanyl has many side effects, including:



    Weakness and fatigue.

    Feelings of elation (euphoria).

    Dry mouth.

    Difficulty urinating.

    Difficulty breathing.

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        Talk with your doctor about using laxatives to prevent constipation.

        You can prevent constipation at home. Make sure you drink enough fluids. Most adults should drink between 8 and 10 glasses of water or noncaffeinated beverages each day. Include fruits, vegetables, and fiber in your diet each day.


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