Restoril (temazepam)

About Restoril

Restoril Side Effects

Restoril Interactions

Restoril Directions

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About Restoril

Restoril is a benzodiazepine sedative, prescribed for short term treatment of insomnia (see Sleep Disorders), with manufacturer's guidelines suggesting reevaluation after 7-10 days. This treatment is not generally recommended for longer than 2-3 weeks.

Restoril is only available by prescription. Do not use this medication with alcohol, narcotic pain medications, or other sedatives.

Restoril Side Effects

Drowsiness is an unavoidable, and intentional, side effect of this medication. Take it only before going to sleep for the night.

Common Side Effects: Dizziness, headache, fatigue, light-headedness, nausea, nervousness, sluggish feeling. After treatment is stopped, one or two nights of 'rebound' insomnia are typical. This effect may be worsened if you stop treatment abruptly after using it for several weeks. Speak to your doctor about the best way to step down your dosage and end Restoril treatment.

Less Common Side Effects: Abdominal pain, agitation, altered sex drive, blurred or altered vision, chest pain, confusion, constipation or diarrhea, cramps, difficult urination, dry mouth, false sense of well-being, fatigue, headache, nausea or vomiting, runny nose, trembling, unusual weakness.

Uncommon to Rare Side Effects: Aggressive behavior, angry outbursts, anxiety, cold or flu-like symptoms, confusion, delusions, depression, excitement, hallucinations, insomnia, involuntary movements, irritability, loss of coordination, low blood pressure, lowered inhibitions (as in intoxication with alcohol), muscle weakness, racing heartbeat, rash or itching, seizures, slurred speech, sores in the mouth, strange behavior, temporary amnesia. Contact your doctor as soon as possible if any of these conditions occur, particularly if you have a history of depression or other personality disorder.

Cautions: Restoril is not for everyone. A history, or present case, of any of the following conditions may be grounds for a doctor to determine that you should try another treatment.

  • Alcohol or drug abuse - may increase likelihood of Restoril dependence
  • Allergic reaction to Restoril, or other benzodiazepine. Always tell your doctor about any allergies before starting a medication, including food and dye reactions.
  • Borderline personality disorder or a history of violent behavior may be contraindications for treatment with this medication.
  • Brain disease - may increase likelihood of side effects from Restoril.
  • Breathing difficulties such as asthma, bronchitis, emphysema, or any other chronic lung disease - Restoril may worsen this condition.
  • Difficulty swallowing - This condition may become more pronounced in children.
  • Epilepsy or seizures - Abruptly starting or stopping treatment with Restoril may increase seizures.
  • Glaucoma - Restoril should not be prescribed to patients with acute narrow-angle glaucoma. Patients receiving treatment for open angle glaucoma should consult their doctor, as Restoril may be an acceptable treatment for them.
  • Hyperactivity - Benzodiazepines may worsen this condition.
  • Kidney or liver problems - More Restoril may end up in your bloodstream if you have a pre-existing kidney or liver condition, increasing the likelihood of side effects.
  • Major Depression - Benzodiazepines may worsen this condition, and are known to increase suicidal ideation in depressed individuals.
  • Myasthenia gravis - This autoimmune disorder characterized by muscle weakness may be aggravated by Restoril treatment.
  • Porphyria - Restoril (temazepam) is listed as an unsafe drug for porphyria, an enzyme deficiency that can cause fragile skin that is sensitive to sunlight, digestive difficulties, anxiety, and reddish-brown urine.
  • Psychosis or other serious mental illness - Restoril has not proved to be an effective treatment for these conditions, and might not be recommended due to potential side effects.
  • Sleep apnea (temporary suspension of breathing during sleep, typically accompanied by snoring) - Restoril may worsen sleep apnea by further relaxing loose tissue in the breathing passages thought to cause the problem. Individuals with sleep apnea should not generally use sedatives as sleep aids. (See Sleep Disorders)

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Restoril Interactions

Restoril should not be combined with all other medications, whether prescription, herbal, or over the counter. This medication is a central nervous system depressant, and should be used cautiously with any other medications that cause drowsiness or sedation. Speak with your doctor or pharmacist if you take, or plan to take, any of the following during treatment. You may wish to have them help you design a medication schedule that prevents certain treatments from interfering with each other, though certain of these drugs should not be used with Restoril at all.

Only your doctor can determine if a medication is safe for you to use during treatment. Speak to a doctor or pharmacist if you should need to start taking another medication (even over the counter treatments) while you are using Restoril.

Restoril Directions

The common recommended dose for Restoril is 15 mg. Though some people may need up to 30 mg, this dose should not be exceeded. Elderly or ill patients may find that a dose of 7.5 mg works for them, though some may tolerate larger doses.

Take Restoril only when you will be able to sleep for 7-8 hours without interruption, to allow it to clear from the body. If this medication is taken when you are travelling, consuming alcohol, or do not have time to sleep, a temporary amnesia may occur for the duration of the drug's presence in the body.

Do not increase your dose of Restoril without instructions from your doctor. While this medication is not considered necessary, you run an increased risk of side effects like rebound insomnia if you miss doses or discontinue use abruptly. If you should miss a dose, do not take another one until the following night when instructed by your doctor. Do not take double doses of this medication.

Do not discontinue treatment abruptly, or without the advice of your doctor. Withdrawal symptoms may range from mild insomnia, to cramps, sweating, and tremor, depending on the length of use and dosage taken. Gradual withdrawal under the guidance of your physician is recommended.

Inform your doctor, dentist, or anesthesiologist that you are taking Restoril before any kind of surgery or medical test. This medication may interfere with certain test results. Restoril should not be combined with certain medications given during surgery.

Store Restoril away from direct light and heat. Store in a dry location; avoid storing it in the bathroom, near sinks, or other areas where it may become damp. Do not use after the expiration date.

Keep Restoril away from children; both when storing it, and when discarding any unused medication.

Restoril was designed to cause drowsiness, and may cause disorientation or temporary amnesia if you remain awake while using it. Do not take it before planning to drive or engage in any other potentially hazardous activity. Take this sedative only as you are preparing to sleep, at a time suggested by your doctor based on your usual bedtime.

Pregnant or nursing women, and individuals under 18 years of age should not use Restoril. Seniors may be more susceptible to undesirable side effects, like sedation the following day or lack of coordination, and should use the smallest possible dose.

 

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Temazepam is manufactured by Geneva and Mylan

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This document is provided for information only. It is not a substitute for consultation with a physician, either to diagnose symptoms or prescribe treatment. Any dosages mentioned are general guidelines only, please follow the directions of your doctor or pharmacist exactly when taking medication. We have made every effort to ensure that this information is accurate, but only your doctor can say if a medication, or drug combination, is safe for you. Information intended for US residents only.
 
     
 
 

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