Bromide

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This page reprints a manufacturer label. Everything below in quotation marks is copied from Description:, published by FDA and retrieved on 2026-09-16. Nothing has been added, reworded or left out of the sections shown. It is the manufacturer’s label, reproduced as published.

This page reprints the FDA label for Description: by Pegasus Laboratories, Inc, a bromide product labelled for dogs and cats. The sections below are copied from that label without change, with the set id and the date it was retrieved from DailyMed. 2 other stored labels carry the same active ingredient and are listed at the end.

The label

Product: Description:. Manufacturer: Pegasus Laboratories, Inc. FDA Structured Product Label set id 2e3a2675-0bfb-4a6a-b645-1db5127dbd41. Label effective 2024-08-19. Retrieved 2026-09-16 from the DailyMed animal label release, and readable on DailyMed.

Indications

K-BroVet potassium bromide is used to treat seizure disorders in dogs. It can be used in addition to therapy with other agents or as the sole anticonvulsant.

Dosage and Administration

Recommended Dosage for K-BroVet Oral Solution: To achieve a serum level of approximately 1 mg/mL, give 120 mg/kg PO daily for 5 days then reduce to 30 mg/kg PO once daily. To achieve a serum level of approximately 1.5 mg/mL, give 160 mg/kg PO for 5 days and then reduce to 40 mg/kg PO once daily thereafter. (R-21) Among dogs responses to bromide may vary, treatment should be tailored to the individual dog, based on serum bromide concentration, success of seizure control, and the observation of adverse effects. Steady state serum concentrations generally take 4 to 5 months in dogs; therapeutic concentrations may be reached before steady state at about 4 weeks after the beginning of treatment, serum bromide concentration may be tested to assess the response to product and, if results are satisfactory , the next testing for steady state serum levels is typically about 4 months. If the dog's serum concentration is within range and the dog is doing well in the therapeutic range , serum concentration may then be tested every 6 to 12 months. Serum bromide is typically evaluated at the end of the loading period, then as described above when an animal is started with a loading dose. Dogs -- An oral dose of 30 mg of Bromide per kg of body weight every twelve hours for 115 days produced a steady state serum concentration of 2.45 mg/mL (range, 1.78 to 2.69 mg/mL) in Beagles fed a diet containing 0.55% chloride. (R-3)

Contraindications

K-BroVet should not be used in animals with a history of hypersensitivity to Bromide or any of the components of the solution or tablets.

Warnings

This medication should be used cautiously in older animals as they will be more susceptible to adverse effects. This medication is not indicated for use in cats. Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian. For Veterinary Use Only Not for Human Use KEEP OUT OF REACH OF CHILDREN AND ANIMALS Possible Side Effects: Dog may experience drowsiness when taking K-BroVet, but this will generally go away after approximately 3 weeks. Increased hunger, thirst, urination, vomiting, constipation, anorexia, and uncoordinated movements may occur with K-BroVet. During the load in dose increased nausea may be experienced. There is no information on the relative frequency of pancreatitis in dogs associated with bromide therapy alone. However, pancreatitis has been reported to be more frequent in dogs on concurrent phenobarbital and bromide therapy than dogs on phenobarbital alone. (R-12) Personality changes have been occasionally reported in dogs on bromide, including attention seeking, irritability or aggression, and aimless pacing. Reproduction/Pregnancy/Lactation: The effects of bromide on canine reproduction have not been studied. Young Dogs: Safety of administering bromide to neonates and young animals has not been evaluated. (R-16-17) Drug Interactions and/or Related Effects: Drug interactions and/or related effects have been selected on the basis of their clinical significance (possible mechanism in parentheses where appropriate) - not necessarily inclusive (* = major clinical significance): Note: Any of the following medications taken in combinations, depending on the amount taken, could also interact with K-BroVet. Medications and foods containing bromide and chloride compete for reabsorption by the kidneys; increased amounts of chloride can promote loss of bromide in the urine, leading to a lowering of serum bromide concentrations: Decreased chloride consumption will promote increased renal reabsorption of bromide. (R-1;2;4;5-7,15) Halothane anesthesia (when inhaled a percentage of halothane is metabolized by dogs to produce bromide, along with other compounds); peak serum concentration occurs within about a day and, in one group of dogs, ranged from 0.04 to 0.088 mg/mL and persisted, with some diminishment, for at least ten days. (R-10;11) Consideration should be given to animals that must have repeated anesthesia or that already require high serum bromide concentration for seizure control. Increased bromide levels due to metabolism of halothane are unlikely to be a significant risk for bromide toxicity in most dogs. Pharmacology: Mechanism of Action/Effect: Bromide's mechanism of action has not been clearly defined. By preferential movement across neuronal membranes via gamma-amino butyric (GABA) - activated chloride channels, bromide may aid in controlling seizures through hyperpolarization of neuronal cell membranes, leading to stabilization and decreased sensitivity to epileptic foci. (R-2; 15) Volume of Distribution: Dogs: 0.45 ± 0.07 L/kg (R-4) Protein binding: Bromide is minimally protein bound. (R-20) Biotransformation: Bromide is not biotransformed by the liver and is eliminated unchanged, primarily by renal clearance. (R-2) Half-life Elimination: Bromide is freely filtered by the glomerulus, but is reabsorbed by the kidneys, in competition with chloride. (R-7) Bromide reabsorption will predominate in the absence of a large chloride load, causing a significantly extended elimination half-life in dogs. (R-4; 5; 7) Increasing chloride intake by an animal on a low chloride diet will decrease the half life of elimination. (R-14;15) Elimination: Renal. Because bromide is widely distributed, minute amounts will also be excreted in saliva, sweat and feces. (R-5;6) Rate of elimination of bromide will increase in dogs that receive a high level of chloride supplementation. (R-4) Overdose: For more information in cases of overdose or unintentional ingestion, contact the American Society for the Prevention of Cruelty to Animals (ASPCA) National Animal Poison Control Center (888-426-4435 or 900-443-000; a fee may be required for consultation) and/or the drug manufacturer. Note: Signs of bromide toxicity are dose-related but dogs differ in their sensitivity. Bromide toxicity has rarely been reported in dogs with serum bromide concentrations of less than 1.5 mg/mL. Signs have been reported in some dogs with relatively low serum concentration (2.75 mg/mL) while not appearing in other dogs with significantly higher concentration (4 mg/mL). (R-3;18) Dogs on concurrent bromide and phenobarbital therapy may be prone to bromide toxicity at lower serum concentrations than when bromide is administered alone. Other physical factors may also play a role in sensitivity. (R-3) Short-term bromide toxicity is considered completely reversible. (R-18) However, mild bromide toxicity can progress to more severe nervous system dysfunction with ongoing high serum concentration of bromide. (R-8) Other species - Bromide toxicity has also been reported in cattle, goats, and horses fed hay that contained bromide ion residue from accidental treatment with methyl bromide. Signs included ataxia, hind limb weakness, joint swelling, and sedation or recumbency. (R-9) Clinical effects of overdose: Clinical signs may appear with serum bromide concentration > 1.5 mg/mL in dogs on bromide therapy alone, but become more common as serum concentration increases, and most common when serum concentration exceeds 4 mg/mL in dogs receiving bromide as the only anticonvulsant (2 to 3 mg/mL in dogs receiving concurrent phenobarbital and bromide). (R-3;18) Ataxia; diarrhea; hematochezia; salvation, excessive; shivering; skin lesions; stupor, progressing to coma and death - Reported with a dose of 200 to 500 mg/kg a day for 4 to 26 weeks. (R-13) Treatment of bromide toxicity . Recommended treatment consist of the following: For dogs on concurrent phenobarbital and bromide therapy with mild sedation, ataxia or hind leg weakness, a 10 to 25% reduction in phenobarbital may resolve the signs within five to seven days. (R-19) For dogs receiving bromide as the only anticonvulsant, K-BroVet may be discontinued for a few days while monitoring serum concentration, to see if mild signs of toxicity will resolve. If necessary, renal excretion of bromide may be accelerated by increasing sodium chloride consumption or administering 0.9% sodium chloride intravenously over twelve hours, depending on the severity of the toxicity. (R-7;8;13) Supportive treatment Continue to monitor

Description

K-BroVet Oral Solution is a butterscotch vanilla flavored solution containing 250 mg/mL of potassium bromide, cyanocobalamin and pyridoxine HCl.

Storage

Store in a tightly sealed container at room temperature (59-86°F).

Other labels for this ingredient

These labels are also stored for the same active ingredient. They are not identical to the one reprinted above, and each is listed by product and set id rather than merged with it.

FDA adverse event reports

The FDA Center for Veterinary Medicine publishes the adverse event reports it receives through openFDA. The counts below are the reports naming bromide as an active ingredient for each species this label names, as returned on 2026-09-16, coded by the VeDDRA reaction term the reporter chose. Reactions are counted per report, so one report can appear under several terms.

These are counts, not rates. Reporting is voluntary, the number of animals treated is not known, and a widely used product accumulates reports for that reason alone. A report records that an event followed a dose; it does not establish that the product caused it. The counts say nothing about how one product compares with another.

Dogs: 415 reports

Reactions most often coded in dogs, 415 reports
VeDDRA reaction termReports
Seizure NOS84
Lack of efficacy - NOS74
Lethargy (see also Central nervous system depression in 'Neurological')46
Ataxia43
Vomiting33
Other abnormal test result NOS31
INEFFECTIVE, SEIZURES23
Diarrhoea21
Elevated serum alkaline phosphatase (SAP)17
Limb weakness17
Cough16
Death by euthanasia16
Emesis16
Increased seizure frequency15
Anorexia14

Outcome as recorded by the reporter: Outcome Unknown 152; Recovered/Normal 136; Ongoing 87; Euthanized 16; Died 14; Recovered with Sequela 9.

Queries: reports, reactions, outcomes. Dataset: openFDA Animal and Veterinary Adverse Event Reports.

Cats: 2 reports

Reactions most often coded in cats, 2 reports
VeDDRA reaction termReports
Cardiac arrest1
Death1
Decreased haematocrit1
Decreased mean corpuscular haemoglobin concentration (MCHC)1
Decreased mean corpuscular volume (MCV)1
Iron deficiency anaemia1
Lack of efficacy - NOS1

Outcome as recorded by the reporter: Died 1; Ongoing 1.

Queries: reports, reactions, outcomes. Dataset: openFDA Animal and Veterinary Adverse Event Reports.

Sources

  • Description:FDA · retrieved 2026-09-16
    Recommended Dosage for K-BroVet Oral Solution: To achieve a serum level of approximately 1 mg/mL, give 120 mg/kg PO daily for 5 days then reduce to 30 mg/kg PO once daily. (Dosage and Administration)
  • openFDA Animal and Veterinary Adverse Event ReportsFDA · retrieved 2026-09-16

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