Protriptyline is used to treat depression. It works to maintain a balance of natural substances in the brain.
Protriptyline is a prescription medication used to treat the symptoms of depression. Protriptyline is in a class of medications called tricyclic antidepressants (TCAs). It works by increasing the levels of certain natural substances in the brain that maintain mental balance.
Protriptyline is available as an oral (by mouth) tablet and is usually taken 3 or 4 times a day.
Common side effects of protriptyline include nausea, vomiting, and dry mouth. Protriptyline can also cause dizziness, drowsiness, and blurred vision. Do not drive or operate heavy machinery until you know how protriptyline affects you.
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Protriptyline Cautionary Labels
Uses of Protriptyline
Protriptyline is a prescription medication used to treat the symptoms of depression in people who are under close medical supervision.
This medication may be prescribed for other uses. Ask your doctor or pharmacist for more information.
Protriptyline Brand Names
Protriptyline may be found in some form under the following brand names:
Protriptyline Drug Class
Protriptyline is part of the drug class:
Side Effects of Protriptyline
Serious side effects have been reported with protriptyline. See the “Protriptyline Precautions” section.
Common side effects of protriptyline include the following:
- dry mouth
- loss of appetite
- weight changes
- stomach pain or cramps
- changes in urination habits
- changes in sex drive
- rining in the ears
- blurred vision
This is not a complete list of protriptyline side effects. Ask your doctor or pharmacist for more information.
Tell your doctor if you have any side effect that bothers you or that does not go away.
Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.
Tell your doctor about all the medicines you take, including prescription and non-prescription medicines, vitamins, and herbal supplements. Especially tell your doctor if you take:
- cisapride (Propulsid) (not available in the U.S.)
- monoamine oxidase (MAO) inhibitors such as isocarboxazid (Marplan), phenelzine (Nardil), selegiline (Eldepryl, Emsam, Zelapar), and tranylcypromine (Parnate)
- amiodarone (Cordarone, Pacerone)
- antihistamines; bupropion (Wellbutrin)
- celecoxib (Celebrex)
- cimetidine (Tagamet)
- doxorubicin (Adriamycin)
- guanethidine (Ismelin)
- ipratropium (Atrovent)
- medications for anxiety, asthma, colds, diabetes, irritable bowel disease, mental illness, motion sickness, Parkinson's disease, seizures, ulcers, or urinary problems
- medications for irregular heartbeat such as flecainide (Tambocor), moricizine (Ethmozine), and propafenone (Rythmol)
- methadone (Dolophine)
- metoclopramide (Reglan)
- other antidepressants
- ranitidine (Zantac)
- reserpine (Serpasil)
- ritonavir (Norvir)
- selective serotonin reuptake inhibitors (SSRIs) such as citalopram (Celexa), fluoxetine (Prozac, Sarafem), fluvoxamine (Luvox), paroxetine (Paxil), and sertraline (Zoloft)
- sedatives or sleeping pills
- terbinafine (Lamisil)
- thyroid medications
- tramadol (Ultram
This is not a complete list of protriptyline drug interactions. Ask your doctor or pharmacist for more information.
Serious side effects have been reported with protriptyline including the following:
- Cardiovascular side effects. Tell your healthcare provider right away if you have some or all of the following symptoms of cardiovascular side effects:
- heart attack
- heart block
- rapid or irregular heartbeat
- changes in blood pressure
- Psychiatric side effects. Tell your healthcare provider right away if you have some or all of the following symptoms of psychiatric side effects:
- Neurological side effects. Tell your healthcare provider right away if you have some or all of the following symptoms of neurological side effects:
- numbness or tingling in arms or legs
- weakness or fatigue
- ringing in the ears
- Allergic reactions. Tell your healthcare provider right away if you have some or all of the following symptoms of an allergic reaction:
- rash, hives, or itching
- swelling or face or tongue
Protriptyline can cause dizziness, drowsiness, and blurred vision. Do not drive or operate heavy machinery until you know how protriptyline affects you.
Do not take protriptyline if you:
- are allergic to protriptyline or any of its ingredients
- have taken a monoamine oxidase inhibitor within the last 14 days
- are taking cisapride
- have recently had a heart attack
Protriptyline Food Interactions
Medications can interact with certain foods. In some cases, this may be harmful and yoru doctor may advise you to avoid certain foods. In the case of protriptyline, there are no specific foods that you must exclude from your diet when receiving this medication.
Before taking protriptyline, tell your doctor about all of your medical conditions. Especially tell your doctor if you:
- are allergic to protriptyline or to any of its ingredients
- have recently had a heart attack
- drink large amouts of alcohol
- are undergoing electroshock therapy
- have an enlarged prostate
- have difficulting urinating
- have a history of mental illness
- have had seizures
- have hyperthyroidism
- have diabetes
Tell your doctor about all the medicines you take including prescription and non-prescription medicines, vitamins, and herbal supplements.
Protriptyline and Pregnancy
Tell your doctor if you are pregnant or plan to become pregnant.
The FDA categorizes medications based on safety for use during pregnancy. Five categories - A, B, C, D, and X - are used to classify the possible risks to an unborn baby when a medication is taken during pregnancy.
Protriptyline has not been classified into one of these categories because safe use in pregnancy has not been established. The use of protriptyline in pregnant women or women who may become pregnant requires that possible benefits be weighed against possible hazards to the mother and child.
Protriptyline and Lactation
Tell your doctor if you are breastfeeding or plan to breastfeed.Safe use of protriptyline during breastfeeding has not been established. The use of protriptyline in nursing women requires that possible benefits be weighed against possible hazards to the mother and child.
Take protriptyline exactly as prescribed.
Protriptyline comes in oral tablet form and is taken 3 or 4 times a day, with or without food.If you miss a dose, take the missed dose as soon as you remember. If it is almost time for the next dose, skip the missed dose and take your next dose at the regular time. Do not take 2 doses of protriptyline at the same time.
Take this medication exactly as prescribed by your doctor. Follow the directions on your prescription label carefully.
The dose your doctor recommends may be based on the following:
- the condition being treated
- other medical conditions you have
- other medications you are taking
- how you respond to this medication
- your age
The recommended initial dose of protriptyline is 15 to 40 mg per day divided into 3 or 4 doses. The maximum recommended dose of protriptyline is 60 mg per day.
If you take too much protriptyline, call your healthcare provider or local Poison Control Center or seek emergency medical attention right away.
If protriptyline is administered by a healthcare provider in a medical setting, it is unlikely that an overdose will occur. However, if overdose is suspected, seek emergency medical attention.
- Store protriptyline at room temperature.
- Keep this and all medications out of the reach of children.
- Avoid prolonged exposure to the sun while taking protriptyline.
Protriptyline FDA Warning
Suicidality and Antidepressant Drugs
Antidepressants increased the risk compared to placebo of suicidal thinking and behavior (suicidality) in children, adolescents, and young adults in short-term studies of major depressive disorder (MDD) and other psychiatric disorders. Anyone considering the use of protriptyline hydrochloride or any other antidepressant in a child, adolescent, or young adult must balance this risk with the clinical need. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24; there was a reduction in risk with antidepressants compared to placebo in adults aged 65 and older. Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide. Patients of all ages who are started on antidepressant therapy should be monitored appropriately and observed closely for clinical worsening, suicidality, or unusual changes in behavior. Families and caregivers should be advised of the need for close observation and communication with the prescriber. Protriptyline hydrochloride is not approved for use in pediatric patients.