

| Dosage | Package | Price per Dose | Price | |
|---|---|---|---|---|
| 25mg | 360 pills | A$1.13 | A$451.77 A$406.59 Best Price | |
| 25mg | 180 pills | A$1.22 | A$243.06 A$218.75 | |
| 25mg | 120 pills | A$1.41 | A$189.04 A$170.14 | |
| 25mg | 90 pills | A$1.61 | A$162.03 A$145.83 | |
| 25mg | 60 pills | A$1.83 | A$122.75 A$110.47 | |
| 25mg | 30 pills | A$3.03 | A$100.65 A$90.58 | |
| 50mg | 360 pills | A$1.46 | A$584.36 A$525.93 | |
| 50mg | 180 pills | A$1.59 | A$319.18 A$287.26 | |
| 50mg | 120 pills | A$1.75 | A$233.24 A$209.92 | |
| 50mg | 90 pills | A$1.99 | A$198.86 A$178.98 | |
| 50mg | 60 pills | A$2.08 | A$137.48 A$123.73 | |
| 50mg | 30 pills | A$2.43 | A$81.00 A$72.90 | |
| 100mg | 360 pills | A$1.99 | A$795.53 A$715.97 Popular | |
| 100mg | 180 pills | A$2.17 | A$432.13 A$388.91 | |
| 100mg | 120 pills | A$2.34 | A$311.81 A$280.63 | |
| 100mg | 90 pills | A$2.61 | A$260.25 A$234.22 | |
| 100mg | 60 pills | A$2.74 | A$181.68 A$163.51 | |
| 100mg | 30 pills | A$3.25 | A$108.01 A$97.21 |
Disclaimer: This information is for reference purposes only and does not replace professional medical advice. Consult a healthcare professional for guidance tailored to individual health needs.
Major depressive disorder and sleep disturbance often occur together in real life care settings. Insomnia, frequent awakenings, and poor sleep quality can worsen mood symptoms and daytime functioning. In clinical practice, medications with sedating properties may be used to help with sleep when symptoms are distressing or impair daily life.
Trazodone belongs to a class of antidepressants sometimes labeled as serotonin antagonists and reuptake inhibitors (SARIs). The medication is used for mood symptoms and, in some patients, to aid sleep when sleep disturbance is present. The choice of treatment depends on a clinical assessment of benefits and risks for the individual patient.
In Australia, medicines are prescribed by a clinician according to local rules and guidelines. The decision to use trazodone may involve consideration of other symptoms, other medicines being taken, and the potential for adverse effects. Always follow the healthcare professional’s instructions and the product information provided with the medicine.
As with any antidepressant or sedating medicine, careful monitoring is advised during the first weeks of treatment and after any dose changes. If concerns arise about sleep, mood, or energy levels, medical advice should be sought promptly.
Desyrel is the brand name for trazodone. Trazodone is an antidepressant that can help improve mood and relieve symptoms of depression in many patients. In addition, it may assist with sleep problems in people who have difficulty staying asleep or falling asleep due to mood or anxiety symptoms.
The exact mechanism of action is not fully understood, but trazodone is thought to influence serotonin pathways in the brain and to have a sedating effect in some people. This combination can support both mood balance and sleep quality in chosen cases, under medical supervision.
The treatment aims are to stabilize mood over the longer term and to improve sleep patterns in a way that supports daytime functioning and well-being. It is important to use the medicine as directed by a clinician and to report any concerns during therapy.
Desyrel is prescribed under local medical rules and may require a prescription depending on country and local regulations. A healthcare professional will determine whether trazodone is appropriate and safe in relation to existing health conditions and current medicines.
Desyrel should not be used by individuals with a known allergy to trazodone or any ingredient in the tablet form. Allergic reactions can involve symptoms such as skin rash, itching, swelling, or breathing difficulties. If any signs of an allergic reaction occur, seek urgent medical help.
Significant active or recent heart rhythm problems may affect safety. A clinician will assess heart health and may request tests or medical history details before starting therapy. In some circumstances, trazodone is not recommended and alternative treatments may be considered.
Severe liver impairment or active liver disease is a contraindication to use without specialist supervision. The liver plays a role in processing many medicines, and liver conditions can alter drug levels and risk. Check with a healthcare professional about safety considerations in liver disease.
Desyrel must not be used in patients with a recent or current certain types of heart attack, or a history of signaling heart rhythm abnormalities that could be worsened by the medicine. This decision requires professional assessment and may vary by patient history and concurrent therapies.
During therapy, monitoring for mood change, sleep pattern, and energy levels is advised. If suicidal thoughts or behaviors appear to worsen, or if new depressive symptoms arise, urgent medical evaluation is essential. Prompt reporting enables timely action and safety adjustment.
Medication effects on blood pressure can occur, especially after starting treatment or increasing the dose. Dizziness or fainting may be more likely on standing, and caution is advised during activities requiring alertness, such as driving. If dizziness is persistent, contact a healthcare professional.
Desyrel may interact with other medicines that affect the central nervous system. Combinations that increase sedation can impair mental alertness and reaction times. Discuss all medicines, including over-the-counter products and supplements, with a clinician before starting or stopping any drug.
Seizure risk is a consideration for some patients, particularly when there is a history of seizures or when combined with other medicines that lower seizure threshold. If new convulsions occur, medical advice should be sought promptly.
Sleepiness or drowsiness is a frequently reported effect, especially early in treatment or after dose changes. Fatigue or lightheadedness may also be described. If these symptoms interfere with daily activities or persist, a clinician should be informed.
Headache and mild dizziness can occur and are usually mild to moderate in severity. Most often these resolve with continued therapy or dose adjustments under medical guidance.
Some individuals may notice changes in blood pressure or heart rate. Vasodilation or a feeling of lightheadedness upon standing may occur, particularly after initiation of therapy or dose adjustments. Medical assessment is advised if symptoms are persistent or concerning.
Fainting or near-fainting episodes are uncommon but require prompt evaluation to exclude other causes and to assess safety during continued use.
Nausea, dry mouth, constipation, or abdominal discomfort may occur. These effects are usually mild and tend to improve with time or with adjustments advised by a healthcare professional.
Gastrointestinal upset should be reported if persistent, severe, or associated with signs of dehydration or reflex changes in appetite or digestion.
Some patients report muscle or joint pain, or tremor in rare cases. If new or worsening symptoms develop, clinical review is recommended to determine if trazodone is the likely cause or if an alternative explanation exists.
Nighttime sedation may contribute to morning grogginess in some individuals. Less commonly, some patients report dry eyes, blurred vision, or changes in sexual function. Any persistent or troublesome symptoms should be discussed with a healthcare professional.
Skin rash, itching, or hives can occur in a minority of patients. Severe skin reactions are rare but require immediate medical attention. Seek guidance if a rash develops or worsens during therapy.
Interaction checks are essential before starting trazodone. Interactions can alter effectiveness or increase the risk of adverse effects. A clinician will review current medicines and may arrange monitoring or alternative therapies if needed.
Prescribed medicines: Certain antidepressants, antipsychotics, sedatives, and medicines that affect the heart or blood pressure can interact with trazodone. A professional assessment ensures that any combination is safe for the individual patient.
Over-the-counter medicines and supplements: Some products, including those used for sleep, anxiety, or allergies, may interact or enhance sedation. It is important to inform the pharmacist or clinician about any non-prescription products being used.
Food and alcohol: Alcohol can potentiate sedation and impair alertness when taken with trazodone. Food generally does not cause dangerous interactions, but it may influence absorption in some individuals. Advice on drinking safely during therapy should be discussed with a clinician.
Medicines that affect serotonin or mood may interact with trazodone. The safety of combination use requires professional assessment due to potential changes in mood, sleep, or blood pressure.
Herbal products or supplements that affect mood, sleep, or blood pressure can interact with trazodone. These interactions may be unpredictable and require medical supervision.
Alcohol consumption can increase sedation and impair driving or operating machinery. In some cases, combining alcohol with trazodone is discouraged. Guidance should be sought from a clinician regarding personal risk and safety limits.
Pregnancy and breastfeeding require careful risk–benefit assessment. If pregnancy occurs or is planned, it is important to discuss treatment options with a clinician. In some situations, alternative therapies or timing strategies may be recommended.
Use in the elderly should consider age-related changes in drug handling and higher likelihood of adverse effects such as dizziness or sedation. Dose adjustments or closer monitoring may be advised by a healthcare professional.
Pediatric use requires specialist judgment. The safety and effectiveness of trazodone in children and adolescents depend on the condition being treated and other clinical factors. A clinician will determine suitability in younger patients.
Always inform the treating clinician about all health conditions, pregnancies, lactation status, and all medicines being taken to support safety and appropriate use.
Desyrel is usually prescribed after a clinical assessment and may require a prescription depending on local rules. The medication is taken as directed by the clinician, with attention to timing relative to meals and bedtime if sleep symptoms are present.
Safety checks include reporting new or worsening symptoms, particularly mood changes, thoughts of self-harm, severe sleepiness, fainting, chest discomfort, or severe allergic reactions. Prompt reporting can prevent complications.
Storage and disposal should follow local guidelines. Medicines should be kept out of reach of children and stored at room temperature in a dry place unless otherwise advised.
Regular follow-up appointments are important to assess effectiveness, tolerability, and any needed adjustments. Do not stop taking trazodone abruptly without medical advice, as withdrawal-like symptoms may occur.
Information in this section aims to address common safety concerns. If questions arise that are not covered here, consult a healthcare professional for personalised guidance.
The following Q&A uses plain language and avoids fixed dosing instructions. For dosing details, refer to the official leaflet or speak with a clinician.
Consideration is given to real-world safety, including interactions, driving safety, and signs when to seek urgent care.
Fainting or dizziness on standing may occur with trazodone. In some cases, monitoring and dose adjustments are advised. If symptoms are persistent or concerning, a clinician should be consulted before continuing treatment.
Alcohol can enhance sedative effects and impair alertness. It is generally advised to limit or avoid alcohol while on trazodone, and to discuss alcohol use with a clinician if needed.
Initial sedation or dizziness can impact reaction times. It is prudent to assess individual tolerance before engaging in activities requiring high alertness. If significant impairment occurs, avoid driving and inform a clinician.
Missed doses may require guidance from a clinician about how to proceed. If an extra dose is taken accidentally, seek professional advice promptly. Do not double up doses without medical instruction.
Routine blood tests are not universally required for trazodone, but monitoring may be indicated depending on health status, other medicines, and presence of liver disease or heart conditions. Follow the clinician’s recommendations for any tests.
Onset of benefit can vary, and some patients notice gradual improvement over weeks. If no improvement is observed or if mood worsens, a clinician should reassess the treatment plan and may adjust therapy or consider alternatives.
Symptoms such as severe allergic reaction (rash with swelling of face or lips, trouble swallowing or breathing), chest pain, severe fainting, or seizures demand urgent medical evaluation. Seek urgent help or contact a healthcare professional immediately if such signs occur.
Herbal products that affect mood, sleep, or blood pressure may interact with trazodone. The safety of combining such products with trazodone is not guaranteed; professional guidance is recommended before use.
Pregnancy safety requires careful evaluation. The potential benefits and risks should be discussed with a clinician, who can tailor advice based on individual circumstances. Do not start or stop treatment without medical advice during pregnancy.
Breastfeeding safety depends on the drug’s presence in breast milk and infant exposure. A clinician will advise whether continuing, adjusting, or stopping therapy is appropriate for the nursing parent and infant.
Official product information and patient leaflets provide detailed safety data, contraindications, and guidance on use. When questions arise, consult the Australian regulatory authority’s materials, accredited healthcare professionals, or the pharmacist.
Pharmacists and doctors can review medication lists for potential interactions, interpret warning signs, and help plan safe use. In Australia, access to a licensed professional for ongoing assessment remains essential during treatment with trazodone.
Patient information leaflets supplied with Desyrel contain the most up-to-date safety information and dosing considerations. If in doubt, check the official leaflet and seek professional advice for personalised recommendations.
In case of unexpected symptoms or concerns about safety, seek prompt medical attention and discuss concerns with a healthcare professional to determine appropriate action.
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