Buspirone 10 Mg Tablets
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Buspirone 10 mg tablets
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains 10 mg buspirone hydrochloride.
Excipients with known effect:
10 mg tablet: 118.9 mg lactose anhydrous/tablet
For the full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
Tablet.
10 mg tablet:
Tablets are white or almost white, oval tablets debossed with ‘ORN 31’ on one side and a score on the other side.
The tablet can be divided into equal doses.
4 CLINICAL PARTICULARS
4.1 Therapeutic indications
Indicated for the symptomatic treatment of anxiety states of clinically relevant severity with the following cardinal symptoms: anxiety, agitation, tension.
4.2 Posology and method of administration
Posology:
The dosage depends on the individual circumstances of the patient.
For adults over 18 years of age:
At the start of the treatment 5 mg buspirone hydrochloride three times daily and this may be increased every two to three days If necessary, the daily dose can be increased to 20-30 mg buspirone hydrochloride divided into several individual doses.
More than 60 mg buspirone hydrochloride per day should not be taken.
A single dose of 30 mg buspirone hydrochloride should not be exceeded.
If buspirone is administered with a potent CYP3A4 inhibitor, the initial dose should be lowered and only increased gradually after medical evaluation (see section 4.5).
Grapefruit juice increases the plasma concentrations of buspirone. Patients taking buspirone should avoid consuming large quantities of grapefruit juice (see section 4.5).
Due to latency of effect patients should be advised not to expect immediate benefit.
If there is no improvement of symptoms within 4-8 weeks, treatment with buspirone should be reconsidered. Treatment benefits and dose should be reevaluated at regular intervals (see section 4.4).
Special patient groups
Renal impairment
In patients with renal impairment (creatinine clearance 20- 49 ml/min/ 1.72 m ) buspirone should be administered with caution and a low dosage, two-times daily is advised. The response and the symptoms of the patients should be evaluated carefully, before an eventual increase of the dosage is made. Buspirone should not be administered to patients with a creatinin clearance < 20 ml/min/1.72 m , especially not to anuretic patients, because of the fact that increased levels of buspirone and its metabolites may occur (see section 4.3,
4.4 and 5.2).
Hepatic impairment
In patients with hepatic impairment buspirone should be used with caution and individual dosages should be titrated with care to reduce the chance of central undesirable effects, which may occur because of high maximum concentrations of buspirone. Increased dosages should be considered carefully and only after 4-5 days experience with the prior dosage (see section 4.4 and 5.2). Buspirone is contraindicated in patients with severe hepatic impairment (see section 4.3).
Age and gender
Current data do not support any modification of the patient's dosage regimen based on age or gender.
Paediatric Patients
Buspirone should not be used in children and adolescents under 18 years of age as the safety and efficacy of buspirone have not been established in this age group (see section 5.1 and 5.2).
Method of administration
Buspirone tablets can be divided into equal doses and must be swallowed with liquid. The bioavailability of buspirone is increased by food. Buspirone should be taken at the same time each day and consistently with or without food.
4.3 Contraindications
Buspirone should not be administered in case of
- Hypersensitivity to the active substance or to any of the excipients listed in section 6.1
- Acute angle closure glaucoma
- Myasthenia gravis
- Epilepsy
- Acute intoxication with alcohol, hypnotics, analgesics, or antipsychotic drugs
- Severe hepatic insufficiency
- Severe renal insufficiency (creatinine clearance <20 ml/min/1.72 m2).
4.4 Special warnings and precautions for use
Please note
Not all states of anxiety require medical treatment. They may also be a result of physical or mental illness and may sometimes be cured by targeted treatment of the underlying disease.
In clinical and experimental studies, there has been no indication that buspirone causes the risk of developing habituation or addiction. Nevertheless, until further clinical experience is gained, the administration should be monitored accordingly. Buspirone should be used with caution in patients with drug dependence.
Buspirone should be used with caution in patients with hepatic or renal impairment (see section 4.2).
Buspirone should not be used in children and adolescents under 18 years of age as the safety and efficacy have not been established in this age group (see sections 5.1 and
5.2).
Because buspirone has no cross-tolerance to benzodiazepines and other sedatives/hypnotics, it will not block the withdrawal symptoms that often occur at the discontinuation of these preparations. Therefore, before starting treatment with buspirone, these medicinal products should be discontinued gradually. This has particular relevance to patients who have taken a medicinal product with calming effect on the CNS for a long time.Careful observation is recommended for the use of buspirone in patients with a history of seizures.
In individual cases, seizures were reported when taking buspirone and SSRIs concurrently (see section 4.5).
A combination of buspirone with MAOIs is not recommended because of the risk of hypertensive reactions (see section 4.5).
The concomitant use of buspirone with other CNS-active drugs should be approached with caution (see section 4.5).
If a long-term medical treatment is necessary, it should be monitored intensively. The need to continue treatment should be periodically reassessed by discontinuation of treatment after a longer period of time (several months).
Psycho- and sociotherapeutic measures should not be neglected during the treatment with buspirone.
Since the mechanism of action of buspirone is not fully known, the long-term toxic effects on the central nervous system or other body systems cannot be predicted. Controlled clinical studies with buspirone have only been performed over a period of six months.
Buspirone tablets contain lactose. Patients with rare hereditary problems of galactose intolerance, the lapp lactase deficiency, or glucose-galactose malabsorption should not take Buspirone tablets.
4.5 Interaction with other medicinal products and other forms of interaction
There are not sufficient data available regarding the concomitant use with other anxiolytics/sedatives and other centrally acting agents (e.g. antipsychotics and antidepressants), as well as antihypertensives, antidiabetics, anticoagulants, contraceptives and cardiac glycosides. Therefore, the concomitant use of buspirone with these medicinal products should be monitored carefully.
Effect of other drugs on buspirone
MAO inhibitors
Co-administration of MAO inhibitors may cause increases in blood pressure. Coadministration of MAO inhibitors and buspirone is therefore not recommended (see section 4.4).
Erythromycin
Concomitant administration of buspirone hydrochloride (10 mg as single dose) and erythromycin (1.5 g once daily for four days) in healthy volunteers increased the plasma concentrations of buspirone (Cmax increased 5-fold and AUC 6-fold), probably due to CYP 3A4 inhibition. If buspirone and erythromycin are to be used in combination, a low dose of buspirone hydrochloride (e.g., 2.5 mg twice daily) is recommended. Subsequent dose adjustments of either drug should be based on clinical response.
Itraconazole
Concomitant administration of buspirone hydrochloride (10 mg as single dose) and itraconazole (200 mg once daily for four days) in healthy volunteers increased the plasma concentrations of buspirone (Cmax increased 13-fold and AUC 19-fold), probably due to CYP 3A4 inhibition. If buspirone and itraconazole are to be used in combination, a low dose of buspirone hydrochloride (e.g., 2.5 mg once daily) is recommended. Subsequent dose adjustments of either drug should be based on clinical response.
Association with precautions of use:
Diltiazem
Concomitant administration of buspirone hydrochloride (10 mg as single dose) and diltiazem (60 mg three times daily) in healthy volunteers increased the plasma concentrations of buspirone (Cmax increased 5.3-fold and AUC 4-fold), probably due to inhibition of CYP 3A4 first-pass metabolism. Enhanced effects and increased toxicity of buspirone may be possible when buspirone is administered with diltiazem. Subsequent dose adjustments of either drug should be based on clinical response.
Verapamil
Concomitant administration of buspirone hydrochloride (10 mg as single dose) and verapamil (80 mg three times daily) in healthy volunteers increased the plasma concentrations of buspirone (Cmax and AUC increased 3.4-fold), probably due to inhibition of CYP 3A4 first-pass metabolism. Enhanced effects and increased toxicity of buspirone may be possible when buspirone is administered with verapamil. Subsequent dose adjustments of either drug should be based on clinical response.
Rifampicin
Rifampicin induces the metabolism of buspirone via CYP3A4. Therefore, concomitant administration of buspirone hydrochloride (30 mg as single dose) and rifampicin (600 mg once daily for 5 days) in healthy volunteers decreased the plasma concentrations (Cmax decreased 84 % and AUC decreased 90 %) and the pharmacodynamic effect of buspirone.
Association to be taken into account:
SSRI
The combination of buspirone and selective serotonin reuptake inhibitors (SSRI) was tested in a number of clinical trials on more than 300,000 patients. Although no severe toxicities were observed, there were rare cases of seizures in patients that took SSRI and buspirone concomitantly.
Separate cases of seizures in patients administered combination therapy with buspirone and SSRIs have been reported from regular clinical use.
Buspirone should be used with caution in combination with serotonergic drugs (including MAOIs, L-tryptophan, triptans, tramadol, linezolid, SSRIs, lithium and St. John’s wort) as there are isolated reports of serotonin syndrome occurring in patients on concomitant SSRI therapy. If this condition is suspected, treatment with buspirone should be immediately discontinued and supportive symptomatic treatment should be initiated.
Protein binding
In vitro buspirone may displace less firmly protein-bound drugs like digoxin. The clinical significance of this property is unknown.
Nefazodone
The coadministration of buspirone hydrochloride (2.5 or 5 mg twice daily) and nefazodone (250 mg twice daily) to healthy volunteers resulted in marked increases in plasma buspirone concentrations (increases up to 20-fold in Cmax and up to 50-fold in AUC) and statistically significant decreases (about 50%) in plasma concentrations of buspirone metabolite, 1-pyrimidinylpiperazine, probably due to CYP 3A4 inhibition. With 5-mg twice daily doses of buspirone hydrochloride, slight increases in AUC were observed for nefazodone (23%) and its metabolites hydroxynefazodone (HO-NEF) (17%) and mCPP (9%). Slight increases in Cmax were observed for nefazodone (8%) and its metabolite HO-NEF (11%).
The side effect profile for subjects receiving buspirone hydrochloride 2.5 mg twice daily and nefazodone 250 mg twice daily was similar to that for subjects receiving either drug alone. Subjects receiving buspirone hydrochloride 5 mg twice daily and nefazodone 250 mg twice daily experienced side effects such as lightheadedness, asthenia, dizziness, and somnolence. It is recommended that the dose of buspirone be lowered when administered with nefazodone. Subsequent dose adjustments of either drug should be based on clinical response.
Grapefruit juice
Concomitant administration of buspirone hydrochloride 10 mg and grapefruit juice (double strength 200 ml for 2 days) in healthy volunteers increased the plasma concentrations of buspirone (Cmax increased 4.3-fold and AUC 9.2-fold). Patients taking buspirone should avoid consuming large quantities of grapefruit juice.
Other inhibitors and inducers of CYP3A4
When administered with a potent inhibitor of CYP3A4, a low dose of buspirone, used cautiously, is recommended. When used in combination with a potent inducer of CYP3A4, e.g. phenobarbital, phenytoin, carbamazepine, St. John’s wort, an adjustment of the dosage of buspirone may be necessary to maintain busprione’s anxiolytic effect.
Flu.voxa.mine
In short-term treatment with fluvoxamine and buspirone doubled buspirone plasma concentrations are observed compared to mono-therapy with buspirone.
Trazadone
Concomitant administration of trazadone showed a 3-6 fold increase of ALT in some patients.
Cimetidine
The concomitant use of buspirone and cimetidine has shown a slight increase in the 1-(2-pyrimidinyl)-piperazine metabolite of Buspirone. Because of the high protein binding of Buspirone (around 95%) caution is advised when drugs with a high protein binding are given concomitantly.
Baclofen, lofexidine, nabilone, antihistamines may enhance any sedative effect.
Effect of buspirone on other drugs
Diazepam
After addition of buspirone to the diazepam dose regimen, no statistically significant differences in the steady-state pharmacokinetic parameters (Cmax, AUC, and Cmin) were observed for diazepam, but increases of about 15% were seen for nordiazepam, and minor adverse clinical effects (dizziness, headache, and nausea) were observed.
Haloperidol
Concomitant administration of haloperidol and buspirone can increase haloperidol serum levels.
Digoxin
In humans, approximately 95% of buspirone is plasma protein bound. In vitro, buspirone does not displace tightly bound drugs (ie warfarin) from serum proteins. However, in vitro, buspirone may displace less firmly protein-bound drugs like digoxin. The clinical significance of this property is unknown.
Warfarin
There are reports on increases in the prothrombin time after the addition of buspirone to a treatment regimen containing warfarin.
Other CNS depressants
The sedative effect of buspirone may be enhanced if taken with other CNS depressants. Therefore, the concomitant use of buspirone with CNS depressant drugs should be monitored carefully.
The sedative effects of buspirone may be enhanced if taken with alcohol. Therefore the concurrent consumption of alcohol should be avoided.
4.6 Pregnancy and lactation
Pregnancy
In some animal studies, large doses of buspirone during pregnancy had adverse effects on survival and on birth and weaning weight, although there was no effect on foetal development. Since the relevance of this finding in humans has not been established, buspirone should be used only if clearly needed during pregnancy.
Lactation
Available toxicological data in animals have shown excretion of buspirone (metabolite) in milk (for details see 5.3). A risk to the suckling child cannot be excluded. Lactation should therefore be discontinued during the treatment with buspirone.
Fertility
No fertility data are available.
4.7 Effects on ability to drive and use machines
It cannot be excluded that buspirone - especially at the beginning of treatment and after a change in dose - but also by normal use affects the capacity of reaction to such extent that it has influence on the ability to drive and use machines.
Studies have shown that buspirone has less sedative effect than other anxiolytics, as it produces no significant psychomotor impairment. However, its effects on the individual patient’s central nervous system are not predictable. Therefore, patients should be warned not to drive or to operate complex machinery until they are relatively sure that their performance is unimpaired by the use of buspirone.
4.8 Undesirable effects
The following frequency categories are used for classification of adverse reactions: Very common (> 1/10)
Common (> 1/100 to- <1/10)
Uncommon (> 1/1,000 to- <1/100)
Rare (> 1/10,000 to <1/1,000)
Very rare (<1/10,000)
Not known (cannot be estimated from the available data)
Blood and lymphatic system disorders
Rare: blood count changes (eosinophilia, leukopenia, thrombocytopenia) Endocrine disorders
Rare: galactorrhoea, gynaecomastia, thyroid dysfunction
Psychiatric disorders
Common: nightmares, drowsiness, insomnia, dizziness, nervousness,
light-headedness, impaired concentration, agitation, anger, hostility, confusion, depression
Uncommon: depersonalisation, hyperacusis, euphoria, dysphoria, urge to move,
anxiety, loss of interest, association disturbances, hallucinations, suicidal thoughts, seizures
Rare: mood swings, claustrophobia, cold intolerance, stupor, slurred
speech, psychosis, transient memory gaps, serotonin syndrome
Nervous system disorders
Uncommon: numbness, abnormal sensations (e.g. tingling, pricking sensation),
loss of coordination, tremors
Rare: extrapyramidal symptoms including early and late dyskinesia,
dystonia and rigidity, parkinsonism, akathisia, restless legs syndrome, slowed reaction time, involuntary movements
Eye disorders
Common: blurred vision
Uncommon: redness of the eyes, itchy eyes, conjunctivitis
Rare: eye pain, photophobia, sensation of pressure on the eyes, tunnel
vision
Ear and labyrinth disorders
Common: tinnitus
Cardiac disorders
Common: nonspecific chest pain
Uncommon: tachycardia/palpitations
Rare: heart failure, heart attack, cardiomyopathy, bradycardia
Vascular disorders
Uncommon: brief episodes of fainting, hypo- or hypertension
Rare: cerebral blood flow disorders
Respiratory, thoracic and mediastinal disorders
Common: sore throat, stuffy nose
Uncommon: significantly increased breathing frequency, shortness of breath, chest
pressure, altered sense of smell
Rare: nosebleeds
Gastrointestinal disorders
Common: nausea, dry mouth, gastrointestinal symptoms, diarrhoea
Uncommon: increased appetite, anorexia, drooling, rectal bleeding, constipation,
flatulence, irritable colon, vomiting
Hepatobiliary disorders
Uncommon: increased liver enzymes
Skin and subcutaneous tissue disorders
Uncommon: oedema, urticaria, flushing, tendency to bruising, hair loss, dry skin,
eczema, vesicula, facial oedema
allergic reactions, small haemorrhages of the skin, acne, nail thinning
Rare:
Musculoskeletal and connective tissue disorders
Uncommon: muscle cramps, muscle pain, muscle tension, joint pain
Rare: muscle weakness
Renal and urinary disorders
Uncommon: lower urinary tract symptoms
Rare: enuresis, nocturia
Reproductive system and breast disorders
Uncommon: menstrual disorders, decreased or increased libido
Rare: amenorrhea, pelvic inflammatory disease, abnormal ejaculation,
impotence
General disorders and administration site conditions
Common: headache, weakness
Uncommon: weight gain, fever, roaring in the head, weight loss, malaise, fatigue,
altered taste, sweating, clammy hands
Rare: alcohol abuse, bleeding disorders, loss of voice, hiccups, burning
tongue
4.9 Overdose
Symptoms of overdose
Mainly the following symptoms have been observed: nausea, vomiting, dizziness, fatigue, pupillary constriction and stomach complaints. Even with daily doses of up to 2,400 mg in humans, no serious complications were observed.
Therapeutic measures in case of an overdose
In addition to general symptomatic treatment, an immediate gastric lavage should be performed in case of intoxication. As in any other cases of an overdose, breathing, pulse and blood pressure should be monitored. A specific antidote is not known. Buspirone is not removed by haemodialysis, the metabolite 1-PP is partially removed by haemodialysis.
5 PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Nervous system; psycholeptics; anxiolytics, azaspirodecandione derivatives.
ATC code: N05BE01.
Buspirone represents the first anxiolytic of the class of active substances known as azaspirones. These are neither chemically nor pharmacologically related to benzodiazepines, barbiturates, or other psychotropic substances.
Buspirone is a complete agonist at presynaptic 5-hydroxytryptamine type-lA receptors and a partial agonist at postsynaptic 5-hydroxytryptamine type-lA receptors in the CNS.
Apparently the adaptive modulations of 5-HT neurotransmission play a key role in the anxiolytic effects of buspirone after repeated administration, which is why there is a delayed onset of action of 2-4 weeks.
The buspirone metabolite 1-[2-pyrimidinyl]-piperazine (1-PP) is a potent 02-antagonist, and as such it has an impact on the noradrenergic system, which can be associated with psycho-stimulatory and antidepressive effects.
The prevention of or dealing with stress-induced behavioral disorders may perhaps be considered as the fundamental characteristic of buspirone and other 5HT1A agonists. In a number of preclinical studies, buspirone had properties that are characteristic of anxiolytics and antidepressants.
Buspirone or 1-PP do not interact with the GABA-benzodiazepine receptor complex. In contrast to benzodiazepines, buspirone showed no signs of hypnotic-sedative, muscle relaxant, anticonvulsant, or alcohol abusive/addictive effects. In contrast to benzodiazepines, it is unlikely that withdrawal symptoms or a rapid rebound of anxiety symptoms will occur after discontinuation of buspirone.
Paediatric population
Placebo-controlled trials, in which 334 patients were treated with buspirone for up to six weeks, have not shown buspirone at doses recommended for adults to be an effective treatment for generalised anxiety disorder in patients less than 18 years.
5.2 Pharmacokinetic properties
Absorption
Buspirone is absorbed rapidly in humans following oral administration, however, the drug undergoes extensive first-pass metabolism with only about 4% of a dose reaching systemic circulation. Peak plasma levels are reached after 60-90 minutes; they were found to be a linear function of the administered dose over the entire therapeutic range.
Distribution
The plasma half-life is 2-3 hours. In plasma, more than 95% of the active ingredient is bound to proteins. Other drugs with high protein binding in blood, such as phenytoin, propranolol and warfarin, are not displaced by buspirone from plasma protein in vitro at clinically relevant buspirone concentrations. At higher concentrations, digoxin is displaced by buspirone in vitro; however, the clinical relevance of this finding is not clear.
Biotransformation
Buspirone is primarily metabolized by oxidation; the involvement of cytochrome P450 3A4 (CYP3A4) was demonstrated in vitro. Several hydroxylated derivatives and two pharmacologically active metabolites, 6-Hydroxybuspiron (6-OHB) and 1-Pyrimidinylpiperazin (1-PP), are produced.
In an animal study investigating the anxiolytic potential, 6-OHB displayed the same activity profile as buspirone.
In healthy volunteers, who received buspirone orally, the plasma concentrations of 6-OHB were approximately 40 times greater than those of buspirone, which leads to the suggestion that mainly this metabolite contributes to the clinical anxiolytic effects.
In animal studies, that have led to the conclusion of anxiolytic potential, the activity of 1-PP is approximately 25% or less compared to the activity of buspirone.
Elimination
The excretion of buspirone and its metabolites is approximately 29-63% in urine and 18-38% in faeces. The elimination of buspirone is reduced in patients with impaired hepatic or renal function. There were no significant differences in the pharmacokinetics of buspirone in relation to age or gender.
Renal impairment
After a single administration to patients with renal insufficiency (creatinin clearance 20-49 ml/min/1.72 m2) a slight increase in the buspirone blood levels was seen, without increase of the half-life time. A single administration to anuretic patients causes an increase in the blood levels of the metabolite 1-pyrimidine/piperazine (1-PP), in which dialysis did not prove to have any influence on the buspirone levels, neither on the 1-PP levels.
Hepatic impairment
As may be expected agents as buspirone used in patients with a reduced liver function show a reduced “first pass effect”. After a single administration to patients with liver cirrhosis, higher maximum concentrations of unchanged buspirone are seen, with an increase in the half life time.
Paediatric population
Plasma concentrations of buspirone and its active metabolite were higher in paediatric patients, compared to adults given equivalent doses.
5.3 Preclinical safety data
In studies with different animal species, a moderate acute toxicity of buspirone hydrochloride was determined. LD50 after oral treatment was 330 - 660 mg/kg BW in rats, 200 - 420 mg/kg BW in mice, about 300 mg/kg BW in dogs, and about 350 mg/kg BW in monkeys. Death mostly occurred immediately after administration of the drug and was accompanied by tonic-clonic seizures, body stiffness and other signs of CNS toxicity.
Studies of toxicity after repeated oral administration of buspirone hydrochloride in rats (up to 160 mg/kg BW/d) and mice (up to 200 mg/kg BW/d) showed dose-related weight loss. Tremor, hyperventilation and tachycardia were occasionally seen in rats, and amyloid deposits in the kidneys and the testicular tissue (ranging to testicular atrophy) and in the gastrointestinal tract were seen in mice.
After repeated oral administration of buspirone in monkeys, a dose-dependent mortality (> 50% at 100 mg/kg BW/d buspirone hydrochloride) and CNS toxicity was reported, including tremors, hypoactivity, catatonia, sedation and abnormal chewing movements.
Organ-specific toxic changes were not observed.
Reproductive toxicity studies in rats and rabbits revealed no evidence of teratogenic or fetotoxic effects of buspirone. In lactating rats, buspirone (metabolite) was excreted in the milk.
In in vitro and in vivo studies, buspirone showed no mutagenic or genotoxic effects.
Long-term studies showed no evidence of carcinogenic effects when buspirone hydrochloride was given to rats (up to 160 mg/kg BW/d for 2 years) and mice (up to 200 mg/kg BW/d for 18 months).
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Lactose monohydrate Silica, colloidal anhydrous
Cellulose, microcrystalline Sodium starch glycolate (type A)
Magnesium stearate
6.2 Incompatibilities
Not applicable.
6.3 Shelf life
3 years
HDPE tablet container additionally:
After first opening: 1 year.
6.4 Special precautions for storage
This medicinal product does not require any special temperature storage conditions. Blister additionally:
Keep the blister in the outer carton in order to protect from light.
6.5 Nature and contents of container
PVC/PVDC-Aluminium blister
Packs of 20, 30, 50, 60, 90 and 100 tablets.
HDPE tablet container of 60 ml closed with a 38-mm, round PP child-resistant, tamper-evident screw cap containing 250 tablets.
Not all pack sizes may be marketed.
6.6 Special precautions for disposal
No special requirements.
MARKETING AUTHORISATION HOLDER
7
Orion Corporation Orionintie 1 FI-02200 Espoo Finland
8 MARKETING AUTHORISATION NUMBER(S)
PL 27925/0069
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
14/08/2012
10 DATE OF REVISION OF THE TEXT
21/06/2013