Tenapam3 mg

Established Use

Tenapam is indicated for the short-term symptomatic treatment of anxiety, including severe, disabling anxiety, tension, and agitation associated with acute emotional or situational stress. Tenapam is intended for short-term use only; current psychiatric guidance does not support routine long-term or continuous use of Tenapam because of the risk of tolerance and dependence.

Adjunctive Use

Tenapam may be used as an adjunct for the short-term symptomatic relief of anxiety-related functional and psychosomatic complaints, such as anxiety-associated irritable bowel syndrome, functional cardiovascular or respiratory symptoms, anxiety-related insomnia, and anxiety accompanying certain organic disorders, when anxiety is a significant contributing component. This adjunctive use of Tenapam should also be limited to the shortest duration necessary.

Each tablet contains Bromazepam INN 3 mg.

Tenapam is a medicine belonging to the benzodiazepine group, used for the short-term relief of anxiety, tension, and related symptoms. Tenapam works by calming overactive signaling in the brain, helping reduce feelings of nervousness and restlessness so that anxiety symptoms become more manageable. Tenapam is intended for short courses of treatment under a doctor's supervision and is not meant for long-term or everyday use. Because Tenapam can cause drowsiness and dependence and interacts with alcohol and other sedating medicines, it should be taken only exactly as prescribed. In Bangladesh, Tenapam is available as a 3 mg oral tablet.

Anxiolytic (Benzodiazepine)

Bromazepam is a benzodiazepine that acts on the central nervous system by binding to a specific site on the GABA-A receptor complex. This binding produces a conformational change that enhances the inhibitory effect of gamma-aminobutyric acid (GABA), the principal inhibitory neurotransmitter in the brain, without directly affecting other neurotransmitter systems. The enhanced GABA-ergic inhibition produced by Bromazepam underlies its anxiolytic, sedative, muscle-relaxant, and anticonvulsant properties. At lower doses, Bromazepam predominantly reduces tension and anxiety, while at higher doses sedative and muscle-relaxant effects of Bromazepam become more prominent.

• Take Tenapam tablets by mouth, exactly as prescribed by your doctor.
• Swallow the Tenapam tablet whole with a glass of water; Tenapam may be taken with or without food.
• Take Tenapam at the same times each day to maintain a steady effect.
• Do not increase the dose of Tenapam or take it more often than prescribed.
• Do not stop taking Tenapam suddenly after regular use; your doctor will advise how to reduce the dose of Tenapam gradually.
• Avoid drinking alcohol while taking Tenapam.
• Do not share your Tenapam prescription with anyone else, even if their symptoms seem similar.

• Opioids (e.g., codeine, tramadol, morphine, other opioid pain relievers or cough medicines): Combining Tenapam with opioids can cause profound sedation, respiratory depression, coma, and death. This combination should be avoided whenever possible; if a physician judges it necessary, the lowest effective doses of Tenapam and the opioid should be used for the shortest possible time, with close monitoring for breathing difficulty or excessive drowsiness. See Precautions and Warnings for full guidance.
• Alcohol: Alcohol enhances the sedative effects of Tenapam and should be avoided during treatment with Tenapam.
• Other central nervous system depressants (antidepressants, antipsychotics, other hypnotics/sedatives, antiepileptics, sedating antihistamines, general anesthetics, muscle relaxants): Concurrent use with Tenapam may enhance central nervous system depression, increasing the risk of excessive sedation and impaired coordination.
• CYP3A4 inhibitors (e.g., azole antifungals such as ketoconazole, macrolide antibiotics, protease inhibitors, certain calcium channel blockers, cimetidine): These drugs can reduce the metabolism of Tenapam and increase its blood levels, potentially requiring a dose reduction of Tenapam.
• Disulfiram: May prolong the elimination of Tenapam and increase its sedative effects.

Common Side Effects

Drowsiness, fatigue, muscle weakness, reduced alertness, confusion, headache, and unsteadiness (ataxia) are common with Tenapam, particularly at the start of treatment or with higher doses, and often lessen with continued use. Short-term memory problems (anterograde amnesia) can also occur with Tenapam.

Serious Side Effects – Seek Medical Attention

Contact a doctor or emergency services if Tenapam causes: severe drowsiness, confusion, or difficulty waking up; slow, shallow, or labored breathing (especially if Tenapam is combined with opioids, alcohol, or other sedatives); paradoxical reactions such as increased agitation, aggression, hallucinations, or unusual excitability; signs of a severe allergic reaction (swelling of the face, lips, or throat, difficulty breathing, rash); or, on stopping Tenapam after prolonged use, withdrawal symptoms such as seizures, severe anxiety, tremor, or confusion.

Pregnancy

The safety of Tenapam during pregnancy has not been established, and Tenapam should generally be avoided during pregnancy unless considered clearly necessary by a physician. Benzodiazepines cross the placenta; use of Tenapam in late pregnancy or during labor has been associated with neonatal hypotonia, reduced respiratory function, and hypothermia in the newborn ("floppy infant syndrome"), and infants born to mothers who used Tenapam or other benzodiazepines regularly in late pregnancy may develop neonatal withdrawal symptoms. If Tenapam has been used during pregnancy, the newborn should be monitored accordingly.

Breastfeeding

Tenapam is excreted into breast milk, and breastfeeding should be avoided during treatment with Tenapam.

• Risk of dependence, tolerance, and withdrawal: Tenapam can cause physical and psychological dependence, which increases with higher doses and longer duration of use, and withdrawal symptoms can appear after as little as one week of regular use of Tenapam. Tenapam should be used for the shortest duration necessary, and treatment should never be stopped abruptly after regular use; abrupt discontinuation of Tenapam can cause withdrawal effects including rebound anxiety, tremor, sweating, confusion, hallucinations, and seizures, particularly after prolonged use. Any reduction or discontinuation of Tenapam should be done gradually and under medical supervision.
• Danger of combining with opioids: Taking Tenapam together with opioid medicines (including opioid pain relievers and cough suppressants) can cause profound sedation, respiratory depression, coma, and death, reflecting a well-documented, serious safety concern with combined benzodiazepine and opioid use. This combination should be reserved for situations with no alternative treatment, using the lowest effective doses of Tenapam and the opioid for the shortest possible time, with close monitoring.
• Sedation and impaired ability to drive or operate machinery: Tenapam can cause drowsiness, impaired coordination, amnesia, and slowed reaction time, which may persist into the next day; patients taking Tenapam should not drive or operate hazardous machinery until they know how Tenapam affects them, and this risk increases substantially if alcohol is also consumed.
• Use only for short-term treatment: Tenapam is intended for short courses of treatment; continuous long-term use of Tenapam is not recommended by current guidance, and the need for continued treatment with Tenapam should be reassessed regularly by a doctor.
• Caution in elderly patients: Elderly patients are more sensitive to the sedative effects of Tenapam and have reduced clearance, increasing the risk of excessive sedation, confusion, unsteadiness, and falls; lower doses of Tenapam are recommended.
• Caution in hepatic and respiratory disease: Tenapam should be used with caution in patients with mild-to-moderate hepatic impairment or compromised respiratory function, as Tenapam is contraindicated in severe hepatic insufficiency, severe respiratory insufficiency, and sleep apnea syndrome.
• Risk of paradoxical reactions: Rarely, Tenapam can cause paradoxical reactions such as increased anxiety, agitation, aggression, or hallucinations, particularly in children, elderly patients, or those with underlying psychiatric conditions; if this occurs, Tenapam should be discontinued under medical guidance.

Overdose with Tenapam commonly causes drowsiness, confusion, slurred speech, and unsteadiness (ataxia), which can progress to impaired reflexes, low blood pressure, respiratory depression, and coma in more severe cases, particularly when Tenapam is taken together with alcohol or other central nervous system depressants. Do not induce vomiting unless specifically directed to do so by a doctor or poison control. If an overdose of Tenapam is suspected, contact emergency medical services or a poison control center immediately, or go to the nearest hospital, taking the medicine packaging if possible. Management of Tenapam overdose is generally supportive; in a hospital setting, flumazenil, a specific benzodiazepine-reversal agent, may be used by medical staff for severe central nervous system depression under close monitoring, but it is not for self-administration.

Store Tenapam according to the instructions on the product label, out of reach of children, and away from moisture and direct light. Do not use Tenapam after the expiry date printed on the pack.

Children

The use of Tenapam in children is not recommended; the safety and efficacy of Tenapam have not been established in the pediatric population.

Elderly

Elderly patients should receive lower doses of Tenapam, as clearance is reduced and the risk of excessive sedation, confusion, unsteadiness, and falls is increased.

Renal Impairment

Tenapam should be used with caution in patients with renal impairment, starting at the lowest effective dose, since specific dose-adjustment data for Tenapam are limited.

Hepatic Impairment

Tenapam should be used with caution and at reduced doses in mild-to-moderate hepatic impairment; Tenapam is contraindicated in severe hepatic insufficiency due to the risk of encephalopathy.

Other Populations

Tenapam should be used with caution in patients with a history of alcohol or drug dependence, and in those with respiratory disease, due to increased sensitivity to the sedative and respiratory-depressant effects of Tenapam.

Treatment with Tenapam should be as short as possible; current guidance generally limits regular use of Tenapam to about 2 to 4 weeks, including a gradual tapering period, with an overall course of Tenapam (including tapering) typically not exceeding 8 to 12 weeks. Continuous long-term use of Tenapam is not recommended, and the need for continued treatment with Tenapam should be reviewed regularly by a doctor.

Benzodiazepine; Anxiolytic/Sedative

Bromazepam binds to a specific benzodiazepine binding site on the GABA-A receptor complex in the central nervous system, producing a conformational change that enhances the effect of gamma-aminobutyric acid (GABA) on chloride channel opening. This action of Bromazepam increases inhibitory neurotransmission, producing anxiolytic, sedative, muscle-relaxant, and anticonvulsant effects.

Tenapam is not recommended for use in children. The safety and efficacy of Tenapam have not been established in the pediatric population, so Tenapam should not be given to children.