Leventa 1 mg/ml Oral Solution for Dogs
Active ingredient: L Thyroxine Sodium
Form
Liquid
Species
Manufacturer
Intervet International B.V.
VMD MA No.
06376/5058
What it's used for
For the long term treatment of thyroid insufficiency in dogs.
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Paying less for L Thyroxine Sodium
-
1
Ask your vet for a written prescription
They must provide one on request. Under the CMA Order the fee is capped at £21 from 2027.
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2
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Prescription required
Your vet must provide a written prescription on request. You can then purchase from any licensed online retailer.
Leventa 1 mg/ml Oral Solution for Dogs — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.
regime have to be tailored individually to each dog. A starting dose rate of
20 microgram L-thyroxine sodium/kg once daily is recommended; this
corresponds to 0.2 ml of the veterinary medicinal product per 10 kg bodyweight.
At re-examination four weeks later, dose adjustment should be performed based
on the clinical response to treatment and thyroid hormone concentration
evaluated 4-6 hours after administration of the veterinary medicinal product.
Further assessment of hormonal responses and dose adjustment may be
repeated at 4 week intervals if required.
A maintenance dose rate between 10 and 40 microgram/kg body weight once
daily is generally sufficient to control the clinical signs of hypothyroidism and to
restore thyroid hormone concentrations to within the reference range. Depending
on the dose rate determined as suitable for the dog and on its body weight, the
volume (in ml) of the veterinary medicinal product to be administered once daily
can be estimated using the following table:
Dosage (microgram/kg)10203040
Body
weight
(kg)
Volume of the veterinary medicinal
product (ml)
50.050.100.150.20100.100.200.300.40150.150.300.450.60200.200.400.600.80250.250.500.751.00300.300.600.901.20350.350.701.051.40400.400.801.201.60450.450.901.351.80500.501.001.502.00
The dose for dogs weighing more than 50 kg should be calculated according to
bodyweight in the same way.
Once a suitable dose rate and regime have been established, it is recommended
to recheck every 6 months that thyroid hormone concentrations are appropriate.
The improvement in clinical signs occurs differentially following the onset of
treatment with L-thyroxine: whilst metabolic signs improve within two weeks after
the onset of treatment, dermatological signs may require 6 weeks or more of
treatment before improvement is seen.
The veterinary medicinal product should be administered at the same time every
day. The absorption of L-thyroxine is influenced by food. In order to achieve
consistent absorption of L-thyroxine, it is recommended to administer L-
thyroxine 2 – 3 hours prior to feeding, which will maximise the degree of
absorption and minimize variation in absorption (see also section 4.3).
If L-thyroxine is administered less than 2 hours before feeding, at or after feeding,
the feed given (type and amount) should be standardized.
Instruction for use of the oral syringe:
Open the bottle. Attach the dosing syringe to the bottle by gently pushing the end
of the syringe onto the insert in the bottle. Turn the bottle/syringe upside down
and draw the solution into the syringe by pulling the plunger out until the edge of
the ring on the end of the plunger coincides with the expected volume or body
weight in kilograms. Turn the bottle/syringe right way up and remove the syringe
from the insert. After administering the veterinary medicinal product, clean the
syringe by flushing with clean water and allow to dry naturally.
(hypoadrenocorticism).
Do not use in cases of hypersensitivity to the active substance or to any of the
excipients.
Rare
(1 to 10 animals / 10,000
animals treated):
Weight loss, Polydipsia
Polyuria
Hyperactivity
Vomiting, Diarrhoea.
Very rare
(<1 animal / 10,000 animals
treated, including isolated
reports):
Polyphagia
Tachycardia
Skin reaction (e.g. scale
)
.
1 Mild to moderate formation.
2 Transient and self-resolving.
Adverse reactions associated with treatment with L-thyroxine sodium are primarily
those of hyperthyroidism due to therapeutic overdose.
Reporting adverse events is important. It allows continuous safety monitoring of a
veterinary medicinal product. Reports should be sent, preferably via a veterinarian,
to either the marketing authorisation holder or the national competent authority via
the national reporting system. See the package leaflet for respective contact
details.
Special precautions for safe use in the target species:
The veterinary medicinal product should be used with caution in dogs with cardiac
disease, diabetes mellitus or treated adrenal insufficiency (hypoadrenocorticism).
For these dogs, gradual introduction of levothyroxine therapy, starting with 25% of
the normal dose and increasing by 25% increments every two weeks until optimal
stabilisation is achieved is recommended.
The clinical diagnosis of hypothyroidism should be confirmed by laboratory tests.
Special precautions to be taken by the person administering the veterinary
medicinal product to animals:
In case of accidental ingestion, seek medical advice immediately and show the
package leaflet or the label to the physician. Note: this veterinary medicinal
product contains a high concentration of
L-thyroxine sodium and may present a risk to humans if ingested.
Wash hands after use.
In case of eye contact, flush immediately with water.
Special precautions for the protection of the environment:
Not applicable.
antacids, e.g. aluminium or magnesium salts or calcium carbonate, or ferrous
sulphate, and sucralfate. Therefore, concomitant administration of veterinary
medicinal product with the above mentioned compounds should be avoided. At
least 2 hours should elapse between administration of veterinary medicinal
product and such products.
The therapeutic response to veterinary medicinal product may be altered by any
compound that influences thyroid hormone metabolism and disposition (e.g. drugs
displacing protein-binding site, modifying serum thyroxine-binding globulin
concentration, or altering hepatic degradation of thyroxine or peripheral conversion
of thyroxine to triiodothyronine). Thus, in case of concomitant administration of
veterinary medicinal product with a compound exhibiting one of these properties, it
is recommended to recheck that thyroid hormone concentrations are appropriate
and to adjust the dose of veterinary medicinal product accordingly if needed.
Conversely, L-thyroxine supplementation may affect the pharmacokinetics and
activity of concurrent therapies. In diabetic dogs treated with insulin, L-thyroxine
supplementation may alter insulin requirements. In dogs with cardiac insufficiency,
therapeutic response to cardiac glycosides may be decreased by L-thyroxine
supplementation. Therefore, if treated with any of these compounds, dogs should
be monitored carefully during initiation of treatment with veterinary medicinal
product.
Please inform your veterinary surgeon if your dog receives any other medication
before or during treatment with veterinary medicinal product.
Store in the original container.
4.
This information is sourced from the official Summary of Product Characteristics (SPC) published by the Veterinary Medicines Directorate (VMD). It is provided for informational purposes only and does not replace professional veterinary advice. Always consult your vet before administering any medication.
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Other Products Containing L Thyroxine Sodium
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Leventa 1 mg/ml Oral Solution for Dogs
POM-VIntervet International B.V.
Soloxine 0.1 mg Tablet
POM-VVirbac
Soloxine 0.2 mg Tablet
POM-VVirbac
Soloxine 0.3 mg Tablet
POM-VVirbac
Soloxine 0.5 mg Tablet
POM-VVirbac
Soloxine 0.8 mg Tablet
POM-VVirbac
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