Zaleplon (Page 7 of 7)

OVERDOSAGE

Signs and Symptoms

Signs and symptoms of overdose effects of CNS depressants can be expected to present as exaggerations of the pharmacological effects noted in preclinical testing. Overdose is usually manifested by degrees of central nervous system depression ranging from drowsiness to coma. In mild cases, symptoms include drowsiness, mental confusion, and lethargy; in more serious cases, symptoms may include ataxia, hypotonia, hypotension, respiratory depression, rarely coma, and very rarely death.

Loss of consciousness, in addition to signs and symptoms consistent with CNS depressants as described above, have been reported following zaleplon overdose. Individuals have fully recovered from zaleplon overdoses of greater than 200 mg (10 times the maximum recommended dose of zaleplon). Rare instances of fatal outcomes following overdose with zaleplon, most often associated with overdose of additional CNS depressants, have been reported.

Recommended Treatment

General symptomatic and supportive measures should be used along with immediate gastric lavage where appropriate. Intravenous fluids should be administered as needed. Animal studies suggest that flumazenil is an antagonist to zaleplon. However, there is no pre-marketing clinical experience with the use of flumazenil as an antidote to a zaleplon overdose. As in all cases of drug overdose, respiration, pulse, blood pressure, and other appropriate signs should be monitored and general supportive measures employed. Hypotension and CNS depression should be monitored and treated by appropriate medical intervention.

Poison Control Center

As with the management of all overdosage, the possibility of multiple drug ingestion should be considered. The physician may wish to consider contacting a poison control center for up-to-date information on the management of hypnotic drug product overdosage.

DOSAGE AND ADMINISTRATION

The dose of zaleplon capsules should be individualized. The recommended dose of zaleplon capsules for most nonelderly adults is 10 mg. For certain low weight individuals, 5 mg may be a sufficient dose. Although the risk of certain adverse events associated with the use of zaleplon capsules appears to be dose dependent, the 20 mg dose has been shown to be adequately tolerated and may be considered for the occasional patient who does not benefit from a trial of a lower dose. Doses above 20 mg have not been adequately evaluated and are not recommended.

Zaleplon capsules should be taken immediately before bedtime or after the patient has gone to bed and has experienced difficulty falling asleep (see PRECAUTIONS). Taking zaleplon capsules with or immediately after a heavy, high-fat meal results in slower absorption and would be expected to reduce the effect of zaleplon capsules on sleep latency (see Pharmacokinetics under CLINICAL PHARMACOLOGY).

Special Populations

Elderly patients and debilitated patients appear to be more sensitive to the effects of hypnotics, and respond to 5 mg of zaleplon capsules. The recommended dose for these patients is therefore 5 mg. Doses over 10 mg are not recommended.

Hepatic insufficiency:

Patients with mild to moderate hepatic impairment should be treated with zaleplon capsules 5 mg because clearance is reduced in this population. Zaleplon capsules are not recommended for use in patients with severe hepatic impairment.

Renal insufficiency:

No dose adjustment is necessary in patients with mild to moderate renal impairment. Zaleplon capsules have not been adequately studied in patients with severe renal impairment.

An initial dose of 5 mg should be given to patients concomitantly taking cimetidine because zaleplon clearance is reduced in this population (see Drug Interactions under PRECAUTIONS).

HOW SUPPLIED

NDC: 71335-1466-1: 30 Capsules in a BOTTLE

NDC: 71335-1466-2: 60 Capsules in a BOTTLE

NDC: 71335-1466-3: 90 Capsules in a BOTTLE

NDC: 71335-1466-4: 20 Capsules in a BOTTLE

NDC: 71335-1466-5: 28 Capsules in a BOTTLE

STORAGE CONDITIONS

Store at 20°C to 25°C (68°F to 77°F) [see USP Controlled Room Temperature]. Dispense in a light-resistant container as defined in the USP.

MEDICATION GUIDE
ZALEPLON (ZAH-le-plon) CAPSULES, USP C-IV

Read this Medication Guide before you start taking zaleplon capsules and each time you get a refill. There may be new information. This Medication Guide does not take the place of talking to your doctor about your medical condition or treatment. You and your doctor should talk about zaleplon capsules when you start taking them and at regular checkups.

What is the most important information I should know about zaleplon capsules?

Zaleplon capsules may cause serious side effects including complex sleep behaviors that may cause serious injury and death. After taking zaleplon capsules, you may get up out of bed while not being fully awake and do an activity that you do not know you are doing (complex sleep behaviors). The next morning, you may not remember that you did anything during the night. These activities may occur with zaleplon capsules whether or not you drink alcohol or take other medicines that make you sleepy.

Reported activities include:

  • driving a car (“sleep-driving”)
  • making and eating food
  • talking on the phone
  • having sex
  • sleep-walking

Important:

1. Take zaleplon capsules exactly as prescribed

  • Do not take more zaleplon capsules than prescribed.
  • Take zaleplon capsules right before you get in bed, not sooner.

2. Do not take zaleplon capsules if you:

  • have ever experienced a complex sleep behavior (such as driving a car, making and eating food, talking on the phone or having sex while not fully awake) after taking zaleplon capsules
  • drink alcohol
  • take other medicines that can make you sleepy. Talk to your doctor about all of your medicines. Your doctor will tell you if you can take zaleplon capsules with your other medicines
  • cannot get a full night’s sleep

3. Stop taking zaleplon capsules and call your doctor right away if you find out that you have done any of the above activities after taking zaleplon capsules.

What are zaleplon capsules?

Zaleplon capsules are a sedative-hypnotic (sleep) medicine. Zaleplon capsules are used in adults for the short-term treatment of the symptom of trouble falling asleep from insomnia. Zaleplon capsules do not treat other symptoms of insomnia which include waking up too early in the morning and waking up often during the night.

Zaleplon capsules are not for children.

Zaleplon capsules are a federally controlled substance (C-IV) because it can be abused or lead to dependence. Keep zaleplon capsules in a safe place to prevent misuse and abuse. Selling or giving away zaleplon capsules may harm others, and is against the law. Tell your doctor if you have ever abused or been dependent on alcohol, prescription medicines or street drugs.

Who should not take zaleplon capsules?

Do not take zaleplon capsules if you are allergic to anything in them. See the end of this Medication Guide for a complete list of ingredients in zaleplon capsules.

Zaleplon capsules may not be right for you. Before starting zaleplon capsules, tell your doctor about all of your health conditions, including if you:

  • have a history of depression, mental illness, or suicidal thoughts
  • have a history of drug or alcohol abuse or addiction
  • have kidney or liver disease
  • have a lung disease or breathing problems
  • are pregnant, planning to become pregnant, or breastfeeding

Tell your doctor about all of the medicines you take including prescription and nonprescription medicines, vitamins and herbal supplements. Medicines can interact, sometimes causing side effects. Do not take zaleplon capsules with other medicines that can make you sleepy.

Know the medicines you take. Keep a list of your medicines with you to show your doctor and pharmacist each time you get a new medicine.

How should I take zaleplon capsules?

  • Take zaleplon capsules exactly as prescribed. Do not take more zaleplon capsules than prescribed for you.
  • Take zaleplon capsules right before you get into bed. Or you can take zaleplon capsules after you have been in bed and have trouble falling asleep.
  • Do not take zaleplon capsules with or right after a meal.
  • Do not take zaleplon capsules unless you are able to get a full night’s sleep before you must be active again.
  • Call your healthcare provider if your insomnia worsens or is not better within 7 to 10 days. This may mean that there is another condition causing your sleep problem.
  • If you take too much zaleplon capsules or overdose, call your doctor or poison control center right away, or get emergency treatment.

What are the possible side effects of zaleplon capsules?

Serious side effects of zaleplon capsules include:

  • getting out of bed while not being fully awake and do an activity that you do not know you are doing. (See “What is the most important information I should know about zaleplon capsules?”)
  • abnormal thoughts and behavior. Symptoms include more outgoing or aggressive behavior than normal, confusion, agitation, hallucinations, worsening of depression, and suicidal thoughts or actions.
  • memory loss
  • anxiety
  • severe allergic reactions. Symptoms include swelling of the tongue or throat, trouble breathing, and nausea and vomiting. Get emergency medical help if you get these symptoms after taking zaleplon capsules.

Call your doctor right away if you have any of the above side effects or any other side effects that worry you while using zaleplon capsules.

Common side effects of zaleplon capsules include:

  • drowsiness
  • lightheadedness
  • dizziness
  • “pins and needles” feeling on your skin
  • difficulty with coordination
  • You may still feel drowsy the next day after taking zaleplon capsules. Do not drive or do other dangerous activities after taking zaleplon capsules until you feel fully awake.
  • You may have withdrawal symptoms when you stop taking zaleplon capsules. Withdrawal symptoms include unpleasant feelings, stomach and muscle cramps, vomiting, sweating, shakiness, and rarely seizures. You may also have more trouble sleeping the first few nights after zaleplon capsules are stopped. The problem usually goes away on its own after 1 or 2 nights.

These are not all the side effects of zaleplon capsules. Ask your doctor or pharmacist for more information.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1800- FDA- 1088.

How should I store zaleplon capsules?

  • Store zaleplon capsules at room temperature between 68° and 77° F (20º to 25ºC).
  • Protect from light.
  • Keep zaleplon capsules and all medicines out of the reach of children.

General Information about zaleplon capsules

  • Medicines are sometimes prescribed for purposes not mentioned in a Medication Guide.
  • Do not use zaleplon capsules for a condition for which they were not prescribed.
  • Do not give zaleplon capsules to other people, even if they have the same condition. They may harm them and it is against the law.

This Medication Guide summarizes the most important information about zaleplon capsules. If you would like more information, talk with your doctor. You can ask your doctor or pharmacist for information about zaleplon capsules that was written for healthcare professionals.

What are the ingredients in zaleplon capsules?

Active Ingredient: zaleplon, USP

Inactive Ingredients: lactose monohydrate, pregelatinized starch, microcrystalline cellulose, silicon dioxide, magnesium stearate, gelatin, titanium dioxide, FD&C blue #1, FD&C red #40, and FD&C yellow #5. Ink constituents are: shellac, dehydrated alcohol, isopropyl alcohol, butyl alcohol, propylene glycol, strong ammonia solution, black iron oxide and potassium hydroxide.

Zaleplon capsules 5 mg – Dark green colored cap and light blue colored body, “size 4” hard gelatin capsules imprinted with “ZLP” on body and “2122” on cap with black ink, filled with white to off white granular powder.

Zaleplon capsules 10 mg — Dark green colored cap and Opaque blue body, “size 4” hard gelatin capsules imprinted with “ZLP” on body and “2130” on cap with black ink, filled with white to off white granular powder.

Rx only

Manufactured for: OrchidPharma, Inc.
Princeton, NJ 08540, USA

Manufactured by: Orchid Healthcare
(A Division of Orchid Pharma Ltd.)
Irungattukottai — 602 117, India

This Medication Guide has been approved by the U.S. Food and Drug Administration.

Revised: September 2019

948026707

Zaleplon 5mg (CIV) Capsule

Label
(click image for full-size original)
ZALEPLON
zaleplon capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:71335-1466(NDC:42043-210)
Route of Administration ORAL DEA Schedule CIV
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ZALEPLON (ZALEPLON) ZALEPLON 5 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
STARCH, CORN
MICROCRYSTALLINE CELLULOSE
SILICON DIOXIDE
MAGNESIUM STEARATE
GELATIN, UNSPECIFIED
TITANIUM DIOXIDE
FD&C BLUE NO. 1
FD&C RED NO. 40
FD&C YELLOW NO. 5
Product Characteristics
Color GREEN (dark green) , blue (light blue) Score no score
Shape capsule Size 14mm
Flavor Imprint Code ZLP;2122
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:71335-1466-1 30 CAPSULE in 1 BOTTLE None
2 NDC:71335-1466-2 60 CAPSULE in 1 BOTTLE None
3 NDC:71335-1466-3 90 CAPSULE in 1 BOTTLE None
4 NDC:71335-1466-4 20 CAPSULE in 1 BOTTLE None
5 NDC:71335-1466-5 28 CAPSULE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090374 06/20/2018
Labeler — Bryant Ranch Prepack (171714327)
Registrant — Bryant Ranch Prepack (171714327)
Establishment
Name Address ID/FEI Operations
Bryant Ranch Prepack 171714327 REPACK (71335-1466), RELABEL (71335-1466)

Revised: 03/2022 Bryant Ranch Prepack

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