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Diazoxide

Dosage Form: oral suspension

Medically reviewed by Drugs.com. Last updated on Jul 1, 2020.

Diazoxide Description

Diazoxide Oral Suspension, USP is a nondiuretic benzothiadiazine derivative taken orally for the management of symptomatic hypoglycemia. The Suspension contains 50 mg of Diazoxide, USP in each milliliter and has a chocolate-mint flavor; alcohol content is approximately 7.29%. Other ingredients: Sorbitol solution, chocolate mint type flavor, propylene glycol, magnesium aluminum silicate, carboxymethycellulose sodium, sodium benzoate, methylparaben, poloxamer 188, propylparaben, FD&C Red No. 40, FD&C Yellow No. 6 and purified water. Hydrochloric acid may be added to adjust pH.

Diazoxide has the following structural formula:


Diazoxide is 7-chloro-3-methyl-2H-1,2,4-benzothiadiazine1,1-dioxide with the empirical formula C8H7CIN2O2S and the molecular weight 230.7. It is a white powder practically insoluble to sparingly soluble in water.

Diazoxide - Clinical Pharmacology


Diazoxide administered orally produces a prompt dose-related increase in blood glucose level, due primarily to an inhibition of insulin release from the pancreas, and also to an extrapancreatic effect. The hyperglycemic effect begins within an hour and generally lasts no more than eight hours in the presence of normal renal function.

Diazoxide decreases the excretion of sodium and water, resulting in fluid retention which may be clinically significant.

The hypotensive effect of Diazoxide on blood pressure is usually not marked with the oral preparation. This contrasts with the intravenous preparation of Diazoxide (see ADVERSE REACTIONS).

Other pharmacologic actions of Diazoxide include increased pulse rate; increased serum uric acid levels due to decreased excretion; increased serum levels of free fatty acids’ decreased chloride excretion; decreased para-aminohippuric acid; (PAH) clearance with no appreciable effect on glomerular filtration rate.


The concomitant administration of a benzothiazide diuretic may intensify the hyperglycemic and hyperuricemic effects of Diazoxide. In the presence of hypokalemia, hyperglycemic effects are also potentiated.

Diazoxide-induced hyperglycemia is reversed by the administration of insulin or tolbutamide. The inhibition of insulin release by Diazoxide is antagonized by alphaadrenergic blocking agents.


Diazoxideis extensively bound (more than 90%) to serum proteins, and is excreted in the kidneys. The plasma half-life following I.V. administration is 28 ± 8.3 hours. Limited data on oral administration revealed a half-life of 24 and 36 hours in two adults. In four children aged four months to six years, the plasma half-life varied from 9.5 to 24 hours on long-term oral administration. The half-life may be prolonged following overdosage, and in patients with impaired renal function.

INDICATIONS & USAGE

Diazoxide Oral Suspension, USP is useful in the management of hypoglycemia due to hyperinsulinism associated with the following conditions:

Adults: Inoperable islet cell adenoma or carcinoma, or extrapancreatic malignancy.

Infants and Children: Leucine sensitivity, islet cell hyperplasia, nesidioblastosis, extrapancreatic malignancy, islet cell adenoma, or adenomatosis. Diazoxide Oral Suspension, USP may be used preoperatively as a temporary measure, and postoperatively, if hypoglycemia persists.

Diazoxide Oral Suspension, US P should be used only after a diagnosis of hypoglycemia due to one of the above conditions has been definitely established. When other specific medical therapy or surgical management either has been unsuccessful or is not feasible, treatment with Diazoxide Oral Suspension, US P should be considered.

Contraindications

The use of Diazoxide Oral Suspension, USP for functional hypoglycemia is contraindicated. The drug should not be used in patients hypersensitive to Diazoxide or to other thiazides unless the potential benefits outweigh the possible risks.

Warnings


The antidiuretic property of Diazoxide may lead to significant fluid retention, which in patients with compromised cardiac reserve, may precipitate congestive heart failure. The fluid retention will respond to conventional therapy with diuretics.

It should be noted that concomitantly administered thiazides may potentiate the hyperglycemic and hyperuricemic actions of Diazoxide (See DRUG INTERACTIONS and ANIMAL PHARMACOLOGY AND/OR TOXICOLOGY).

Ketoacidosis and nonketotic hyperosmolar coma have been reported in patients treated with recommended doses of Diazoxide Oral Suspension, USP usually during intercurrent illness. Prompt recognition and treatment are essential (See OVERDOSAGE), and prolonged surveillance following the acute episode is necessary because of the long drug half-life of approximately 30 hours. The occurrence of these serious events may be reduced by careful education of patients regarding the need for monitoring the urine for sugar and ketones and for prompt reporting of abnormal findings and unusual symptoms to the physician. Transient cataracts occurred in association with hyperosmolar main an infant, and subsided on correction of the hyper-osmolarity. Cataracts have been observed in several animals receiving daily doses of intravenous or oral Diazoxide.

The development of abnormal facial features in four children treated chronically (>4 years) with Diazoxide Oral Suspension, USP for hypoglycemia hyperinsulinism in the same clinic has been reported.

Pulmonary Hypertension in Neonates and Infants

There have been postmarketing reports of pulmonary hypertension occurring in infants and neonates treated with Diazoxide. The cases were reversible upon discontinuation of the drug. Monitor patients, especially those with risk factors for pulmonary hypertension, for respiratory distress and discontinue Diazoxide if pulmonary hypertension is suspected.

Precautions

GENERAL PRECAUTIONS

Treatment with Diazoxide Oral Suspension, USP should be initiated under close clinical supervision, with careful monitoring of blood glucose and clinical response until the patient’s condition has stabilized. This usually requires several days. If not effective in two to three weeks, the drug should be discontinued.

Prolonged treatment requires regular monitoring of the urine for sugar and ketones, especially under stress conditions, with prompt reporting of any abnormalities to the physician. Additionally, blood sugar levels should be monitored periodically by the physician to determine the need for dose adjustment.

The effects of Diazoxide on the hematopoietic system and the level of serum uric acid should be kept in mind; the latter should be considered particularly in patients with hyperuricemia or a history of gout.

In some patients, higher blood levels have been observed with the oral suspension than with the capsule formulation of Diazoxide. Dosage should be adjusted as necessary in individual patients if changed from one formulation to the other.

Since the plasma half-lifeof Diazoxide is prolonged in patients with impaired renal function, a reduced dosage should be considered. Serum electrolyte levels should also be evaluated for such patients.

The antihypertensive effect of other drugs may be enhanced by Diazoxide Oral Suspension, USP and this should be kept in mind when administering it concomitantly with antihypertensive agents. Because of the protein binding, administration of Diazoxide Oral Suspension, USP with coumarin or its derivatives may require reduction in the dosage of the anticoagulant, although there has been no reported evidence of excessive anticoagulant effect. In addition, Diazoxide may possibly displace bilirubin from albumin; this should be kept in mind particularly when treating newborns with increased bilirubinemia.

Pulmonary hypertension has been reported in neonates and young infants treated with Diazoxide. (see WARNINGS)

INFORMATION FOR PATIENTS

During treatment with Diazoxide Oral Suspension, USP the patient should be advised to consult regularly with the physician and to cooperate in the periodic monitoring of his condition by laboratory tests. In addition, the patient should be advised:

  • to take the drug on a regular schedule as prescribed, not to skip doses, not to take extra doses;
  • not to use this drug with other medications unless this is done with the physician’s advice;
  • not to allow anyone else to take this medication;
  • to follow dietary instructions;
  • to report promptly any adverse effects (i.e., increased urinary frequency, increased thirst, fruity breath odor);
  • to report pregnancy or to discuss plans for pregnancy.

LABORATORY TESTS

The followingprocedures may be especiallyimportant in patientmonitoring (not necessarilyinclusive); blood glucosedeterminations (recommendedatperiodicintervals inpatients takingDiazoxideorallyfortreatment of hypoglycemia,untilstabilized);bloodureanitrogen(BUN)determinations and creatinineclearancedeterminations;hematocritdeterminations;platelet count determinations;total and differentialleukocytecounts;serumaspartateaminotransferase(AST)leveldeterminations;serumuricacidleveldeterminations; and urinetestingforglucose and ketones (in patients beingtreatedwithDiazoxideforhypoglycemia,semiquantitativeestimation of sugar and ketones in serumperformed by the patientandreported to the physicianprovides frequentandrelativelyinexpensivemonitoring of the condition).

DRUG INTERACTIONS

SinceDiazoxideis highly bound to serumproteins,it may displaceothersubstances whicharealso bound to protein,such as bilirubin or coumarin and its derivatives,resulting in higher blood levels of thesesubstances.Concomitantadministration of oralDiazoxideanddiphenylhydantoinmayresult in a loss of seizurecontrol.Thesepotentialinteractions must be consideredwhenadministeringDiazoxideCapsules or Suspension.

The concomitantadministration of thiazides or othercommonlyuseddiuretics may potentiate the hyperglycemic and hyperuricemiceffects of Diazoxide.

DRUG & OR LABORATORY TEST INTERACTIONS

The   hyperglycemic  and hyperuricemic   effects of   Diazoxide   preclude   proper   assessment of   these   metabolic   states. Increased renin secretion, IgG concentrations and decreased   cortisol secretions have   also been noted. Diazoxide   inhibits glucagon-stimulated   insulin   release  and   causes a   false-negative   insulin response  to glucagon.

CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY

No long-term animal dosing study has been done to evaluate the carcinogenic potential of Diazoxide. No laboratory study of mutagenic potential or animal study of effects on fertility has been done.

PREGNANCY


PregnancyCategory C:


Reproductionstudies using the oral preparation in rats haverevealedincreasedfetalresorptions anddelayedparturition, as well as fetalskeletalanomalies;evidence of skeletal and cardiacteratogeniceffects in rabbits has been noted withintravenous administration.The drug has alsobeendemonstrated to cross the placentalbarrier in animals and to causedegeneration of the fetalpancreaticbetacells (SeeANIMALPHARMACOLOGYAND/ORTOXICOLOGY).Sincethere are no adequate data on fetal effects of this drug when given to pregnant women, safety in pregnancy has not been established. When the use of Diazoxide oral suspension, USP is considered, the indications should be limited to those specified above for adults (See INDICATIONS AND USAGE), and the potential benefits to the mother must be weighed against possible harmful effects to the fetus.
Non-teratogeniceffects:

Diazoxidecrosses the placentalbarrier and appears in cord blood.Whengiven to the motherprior to deliveryof the infant,the drug may produce fetal or neonatalhyperbilirubinemia,thrombocytopenia,alteredcarbohydratemetabolism, and possibly other sideeffects thathaveoccurred in adults.

Alopeciaand hypertrichosis lanuginosahaveoccurred in infants whosemothers received oral Diazoxide during the last19 to 60 daysofpregnancy.

LABOR & DELIVERY

Since   intravenous administration of  the  drug  during   labor may   cause   cessation  of  uterine  contractions, and  administration  of  oxytocic agents  may  be  required  to reinstate labor, caution is advised in administering  Diazoxide oral suspension, USP at   that  time.

NURSING MOTHERS

Information  is  not available   concerning  the   passage  of   Diazoxide  in breast   milk. Because   many   drugs  are   excreted in human   milk and because  of  the   potential for adverse   reactions from Diazoxide  in   nursing   infants, a   decision   should be   made   whether to discontinue   nursing  or to discontinue  the   drug,  taking  into   account  the   importance  of  the   drug  to the   mother.

PEDIATRIC USE

(See   INDICATIONS AND USAGE).

Adverse Reactions


Frequent and Serious:

Sodium and fluid retention is most common in young infants and in adults and may precipitate congestive heart failure in patients with compromised cardiac reserve. It usually responds to diuretic therapy (See DRUG INTERACTIONS).

Infrequent but Serious:
Diabetic ketoacidosis and hyperosmolar nonketotic coma may develop very rapidly. Conventional therapy with insulin and restoration of fluid and electrolyte balance is usually effective if instituted promptly. Prolonged surveillance is essential in view of the long half-life of Diazoxide oral suspension, USP (See OVERDOSAGE).


Other frequent adverse reactions:

Hirsutism of the lanugo type, mainly on the forehead, back and limbs, occurs most commonly in children and women and may be cosmetically unacceptable. It subsides on discontinuation of the drug.

Hyperglycemiaor glycosuria may require reduction in dosage in order to avoid progression to ketoacidosis or hyperosmolar coma.

Gastrointestinal intolerancemay include anorexia, nausea, vomiting, abdominal pain, ileus, diarrhea, transient loss of taste.

Tachycardia, palpitations, increased levels of serum uric acid are common.

Thrombocytopenia with or without purpura may require discontinuation of the drug. Neutropenia is transient, is not associated with increased susceptibility to infection, and ordinarily does not require discontinuation of the drug. Skin rash, headache, weakness, and malaise may also occur.

Other adverse reactions which have been observed are:

Cardiovascular: hypotension occurs occasionally, which may be augmented by thiazide diuretics given concurrently. A few cases of transient hypertension, for which no explanation is apparent, have been noted. Chest pain has been reported rarely. Pulmonary hypertension has been reported in neonates and young infants (see WARNINGS).

Hematologic: eosinophilia; decreased hemoglobin / hematocrit; excessive bleeding, decreased IgG.
Hepato-renal: increased AST, alkaline phosphatase; azotemia, decreased creatinine clearance, reversible nephrotic syndrome, decreased urinary output, hematuria, albuminuria. Neurologic: anxiety, dizziness, insomnia, polyneuritis, paresthesia, pruritus, extrapyramidal signs.

Ophthalmologic: transient cataracts, subconjunctival hemorrhage, ring scotoma, blurred vision, diplopia, lacrimation. Skeletal, integumentary; monilial dermatitis, herpes, advance in bone age; loss of scalp hair. Systemic: fever, lymphadenopathy.Other; gout acute pancreatitis/pancreatic necrosis, galactorrhea, enlargement of lump in breast.

Overdosage

An overdosage of Diazoxide oral suspension, USP causes marked hyperglycemia which may be associated with ketoacidosis. It will respond to prompt insulin administration and restoration of fluid and electrolyte balance. Because of the drug’s long half-life (approximately 30 hours), the symptoms of overdosage require prolonged surveillance for periods up to seven days until the blood sugar level stabilizes within the normal range. One investigator reported successful lowering of Diazoxide blood levels by peritoneal dialysis in one patient and by hemodialysis in another.

DOSAGE & ADMINISTRATION


Patients should be under close clinical observation when treatment with Diazoxide oral suspension, USP isinitiated. The clinical response and blood glucose level should be carefully monitored until the patient’s condition has stabilized satisfactory; in most instances, this may be accomplished in several days. If administration of Diazoxide oral suspension, USP is not effective after two or three weeks, the drug should be discontinued.

The dosage of Diazoxide oral suspension, USP must be individualized based on the severity of the hypoglycemic condition and the blood glucose level and clinical response of the patient. The dosage should be adjusted until the desired clinical and laboratory effects are produced with the least amount of the drug. Special care should be taken to assure accuracy of dosage in infants and young children.

Adults and children:

The usual daily dosage is 3 to 8 mg/kg, divided into two or three equal doses every 8 or 12 hours. In certain instances, patients with refractory hypoglycemia may require higher dosages. Ordinarily, an appropriate starting dosage is 3 mg/kg/day, divided into three equal doses every 8 hours. Thus an average adult would receive a starting dosage of approximately 200 mg daily.

Infants and newborns: The usualdailydosage is 8 to 15 mg/kgdivided into two or threeequaldoses every 8 to 12 hours.Anappropriatestartingdosage is 10 mg/kg/day, divided into threeequaldosesevery 8 hours.

ANIMAL PHARMACOLOGY & OR TOXICOLOGY


Oral Diazoxide in the mouse, rat, rabbit, dog, pig, and monkey produces a rapid and transient rise in blood glucose levels. In dogs, increased blood glucose is accompanied by increased free fatty acids, lactate, and pyruvate in the serum. In mice, a marked decrease in liver glycogen and an increase in the blood urea nitrogen level occur.

In acute toxicity studies the LD50 for oral Diazoxide suspension is >5000 mg/kg in the rat, >522 mg/kg in the neonatal rat, between 1900 and 2572 mg/kg in the mouse, and 219 mg/kg in the guinea pig. Although the oral LD 50 was not determined in the dog, a dosage of up to 500 mg/kg was well tolerated.

In subacute oral toxicity studies, Diazoxide at 400 mg/kg in the rat produced growth retardation, edema, increases in liver and kidney weights, and adrenal hypertrophy. Daily dosages up to 1080 mg/kg for three months produced hyperglycemia, an increase in liver weight and an increase in mortality. In dogs given oral Diazoxide at approximately 40 mg/kg/day for one month, no biologically significant gross or microscopic abnormalities were observed. Cataracts, attributed to markedly disturbed carbohydrate metabolism, have been observed in a few dogs given repeated daily doses of oral or intravenous Diazoxide. The lenticular changes resembled those which occur experimentally in animals with increased blood glucose levels. In chronic toxicity studies, rats given a daily dose of 200 mg/kg Diazoxide for 52 weeks had a decrease in weight gain and an increase in heart, liver, adrenal and thyroid weights. Mortality in drug-treated and control groups was not different. Dogs treated with Diazoxide at dosages of 50, l00, and 200 mg/kg/day for 82 weeks had higher blood glucose levels than controls. Mild bone marrow stimulation and increased pancreas weights were evident in the drug-treated dogs; several developed inguinal hernias, one had a testicular seminoma, and another had a mass near the penis. Two females had inguinal mammary swellings. The etiology of these changes was not established. There was no difference in mortality between drug-treated and control groups. In a second chronic oral toxicity study, dogs given milled Diazoxide at 50, l00, and 200 mg/kg/day had anorexia and sever weight loss, causing death in a few. Hematologic, biochemical, and histologic examination did not indicate any cause of death other than inanition. After one year of treatment, there is no evidence of herniation or tissue swelling in any of the dogs.

When Diazoxide was administered at high dosages concomitantly with either chlorothiazide to rats or trichlormethiazide to dogs, increased toxicity was observed. In rats, the combination was nephrotoxic; epithelial hyperplasia was observed in the collecting tubules. In dogs, a diabetic syndrome was produced which resulted in ketosis and death. Neither of the drugs given alone produced these effects.

Although the data are inconclusive, reproduction and teratology studies in several species of animals indicate that Diazoxide, when administered during the critical period of embryo formation, may interfere with normal fetal development, possibly through altered glucose metabolism. Parturition was occasionally prolonged in animals treated at term. Intravenous administration of Diazoxide to pregnant sheep, goats, and swine produced in the fetus an appreciable increase in blood glucose level and degeneration of the beta cells of the Islets of Langerhans. The reversibility of these effects was not studied.

How is Diazoxide Supplied

Diazoxide Oral Suspension, USP 50 mg/mL, a chocolate-mint flavored suspension; bottle of 30 mL (NDC 0254-1010-19), with dropper calibrated to deliver 10, 20, 30, 40 and 50 mg Diazoxide, USP.

Shake well before each  use.  Protect  from  light.  Store  in  carton  until contents are used. Store in light resistant container as defined in the USP. Store Diazoxide Oral Suspension, USP at 25°C (77°F), excursions permitted to 15°-30°C (59-86°F).  [See  USP  Controlled  Room  Temperature].

Rx only

Manufactured by:

Novitium Pharma LLC

70 Lake Drive, East Windsor New Jersey 08520

Distributed by:

Par Pharmaceutical Inc.,

Chestnut Ridge, NY 10977

Issued: 07/2020

OS1010-01-16-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Carton Label for Diazoxide Oral Suspension, USP


Container label for Diazoxide Oral Suspension, USP

Diazoxide 
Diazoxide suspension
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0254-1010
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Diazoxide (Diazoxide) Diazoxide 50 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
SORBITOL  
PROPYLENE GLYCOL  
CARBOXYMETHYLCELLULOSE SODIUM  
SODIUM BENZOATE  
METHYLPARABEN  
POLOXAMER 188  
PROPYLPARABEN  
FD&C RED NO. 40  
FD&C YELLOW NO. 6  
WATER  
ALCOHOL  
HYDROCHLORIC ACID  
MAGNESIUM ALUMINUM SILICATE  
Product Characteristics
Color      Score     
Shape Size
Flavor CHOCOLATE (Chocolate-mint) Imprint Code
Contains     
Packaging
# Item Code Package Description
1 NDC:0254-1010-19 1 BOTTLE, DROPPER in 1 CARTON
1 30 mL in 1 BOTTLE, DROPPER
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA210799 07/21/2020
Labeler - Par Pharmaceutical, Inc (092733690)
 
Par Pharmaceutical, Inc

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