Sinequan

Generic Name: Sinequan

What is Sinequan?

Is it safe to use this drug if I am pregnant or become pregnant during my treatment. Animal studies for this drug have not produced any conclusive evidence of negative effects during pregnancy or for newborns. Doxepin, the active drug in Sinequan, can be excreted into breast milk for nursing mothers. Currently, there is no body of research that determines the safety of this drug for use during pregnancy, however, a thorough risk assessment should be performed between you and your doctor if you are pregnant or become pregnant.

The potential treatment benefits should outweigh the risks if treatment with this drug is pursued during pregnancy. Find a Therapist Advanced Search googletag. Click here for Health Professional Information NOTE: Your browser is not set to use our search feature.

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Interactions for this medication include:Treatment with this drug should not be stopped suddenly. Withdrawal symptoms may be severe and include:If you need to stop taking this medication, please work out a safe plan with your health care provider to slowly taper off your dosage.

This will reduce the occurrence and overall severity of withdrawal symptoms. For information on GoodTherapy. Home Terms of Service Privacy Policy Sitemap Subscribe to The Good Therapy Blog Search our Therapist Directory GoodTherapy. How Does Sinequan Work. Chemistry of Sinequan Dosage FAQs Possible Side Effects Precautions and Warnings Drug Interactions How to Safely Withdraw How Does Sinequan Work.

Chemistry of Sinequan Sinequan is a dibenzoxepin tricyclic compound with a melting point of 25 degrees Celsius. Dosage FAQs What is a normal dose of this medication. The dosage ranges from 25 to 300 mg per day orally. It can be administered in a single dose of 150 mg twice per day. If a person has liver impairment, a 3 mg dose should be administered about 30 minutes before bedtime.

How should I take Sinequan?

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Doxepin is one of these drugs.

What should I avoid while taking Sinequan?

It may also be used for other conditions as determined by your doctor. Some medical conditions may interact with Sinequan. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:Some MEDICINES MAY INTERACT with Sinequan. Tell your health care provider if you are taking any other medicines, especially any of the following:This may not be a complete list of all interactions that may occur. Ask your health care provider if Sinequan may interact with other medicines that you take.

Check with your health care provider before you start, stop, or change the dose of any medicine. Use Sinequan as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Sinequan side effects

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Side effects of medications Health Professionals A-Z Index of PI What is a PI. Doxepin Adapin, Sinequan, Zonalon In Canada Triadapin Doxepin Adapin, Sinequan, Zonalon is an antidepressants, used in the treatment of many types of depression: Doxepin Adapin, Missed Dose s : If within one hour take, if over an hour skip and then continue on your normal schedule. If you only take at this drug at bedtime and miss a dose, do not take in the morning.

Never Take a Double Dose. If stopped abruptly withdrawal syndromes have been reported with his medicine. Do not take this drug if planning to become pregnant.

Common Sinequan ide effects may include:

  • Your doctor may occasionally change your dose to make sure you get the best results.

  • I don't have any side effects now.

  • If signs of toxicity occur at any time during this period, extended monitoring is recommended.

  • Families and caregivers of patients should be advised to look for the emergence of such symptoms on a day-today basis, since changes may be abrupt.

The possibility of development of withdrawal symptoms upon abrupt cessation of treatment after prolonged SINEQUAN administration should be borne in mind. These are not indicative of addiction and gradual withdrawal of medication should not cause these symptoms. Poor metabolizers have higher than expected plasma concentrations of tricyclic antidepressants TCAs when given usual doses. Depending on the fraction of drug metabolized by P450 2D6, the increase in plasma concentration may be small, or quite large 8-fold increase in plasma AUC of the TCA.

Where can I get more information?

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