Hydroxyzine Product Monograph

RECENT MAJOR LABEL CHANGES

Sections or subsections that are not applicable at the time of authorization are not listed.

RECENT MAJOR LABEL CHANGES..............................................................................................2

PART I: HEALTH PROFESSIONAL INFORMATION .......................................................................4

1 INDICATIONS ................................................................................................................4

1.1 Pediatrics ............................................................................................................4

1.2 Geriatrics.............................................................................................................4

2 CONTRAINDICATIONS ...................................................................................................4

4 DOSAGE AND ADMINISTRATION...................................................................................5

4.1 Dosing Considerations .........................................................................................5

4.2 Recommended Dose and Dosage Adjustment.......................................................5

4.5 Missed dose ........................................................................................................5

5 OVERDOSAGE ...............................................................................................................6

6 DOSAGE FORMS, STRENGTHS, COMPOSITION AND PACKAGING ...................................6

7 WARNINGS AND PRECAUTIONS ....................................................................................7

7.1 Special Populations ..............................................................................................9

7.1.1 Pregnant Women .......................................................................................... 9

7.1.2 Breast-feeding............................................................................................... 9

7.1.3 Pediatrics ...................................................................................................... 9

7.1.4 Geriatrics ...................................................................................................... 9

8 ADVERSE REACTIONS .................................................................................................. 10

8.1 Adverse Reaction Overview................................................................................ 10

8.5 Post-Market Adverse Reactions.......................................................................... 10

9 DRUG INTERACTIONS.................................................................................................. 10

9.1 Serious Drug Interactions ................................................................................... 10

9.3 Drug-Behavioural Interactions............................................................................ 11

9.4 Drug-Drug Interactions ...................................................................................... 11

9.5 Drug-Food Interactions ...................................................................................... 12

9.6 Drug-Herb Interactions ...................................................................................... 12

9.7 Drug-Laboratory Test Interactions ...................................................................... 12

10 CLINICAL PHARMACOLOGY ......................................................................................... 12

11 STORAGE, STABILITY AND DISPOSAL ........................................................................... 12

12 SPECIAL HANDLING INSTRUCTIONS............................................................................. 13

PART II: SCIENTIFIC INFORMATION ........................................................................................ 14

13 PHARMACEUTICAL INFORMATION.............................................................................. 14

14 CLINICAL TRIALS.......................................................................................................... 14

15 MICROBIOLOGY .......................................................................................................... 14

16 NON-CLINICAL TOXICOLOGY ....................................................................................... 14

17 SUPPORTING PRODUCT MONOGRAPHS...................................................................... 14

PATIENT MEDICATION INFORMATION ................................................................................... 15

PART I: HEALTH PROFESSIONAL INFORMATION

1 INDICATIONS

HYDROXYZINE (hydroxyzine hydrochloride) is indicated in adults for:

• Management of anxiety.
• Pre-medication, such as preparation for dental procedures.
• Management of pruritus due to allergic conditions such as chronic urticaria and atopic and contact dermatoses.
• Control of nausea and vomiting, excluding nausea and vomiting of pregnancy (see 2 CONTRAINDICATIONS).

1.1 Pediatrics

HYDROXYZINE is indicated in children for:

• Pre-medication, such as preparation for dental procedures.
• Management of pruritus due to allergic conditions such as chronic urticaria and atopic and contact dermatoses.
• Control of nausea and vomiting, excluding nausea and vomiting of pregnancy (see 2 CONTRAINDICATIONS).

1.2 Geriatrics

Evidence from clinical experience suggests that use in the geriatric population is associated with differences in safety or efficacy.

2 CONTRAINDICATIONS

HYDROXYZINE is contraindicated:

• In patients who are hypersensitive to hydroxyzine hydrochloride, cetirizine, other piperazine derivatives, aminophylline or ethylenediamine, or to any ingredient in the formulation, including any non-medicinal ingredient, or component of the container. For a complete listing, see 6 DOSAGE FORMS, STRENGTHS, COMPOSITION AND PACKAGING.
• In patients with history of QT prolongation and/or torsade de pointes, including congenital long QT syndromes; history of cardiac arrhythmias; significant electrolyte imbalance (hypokalemia, hypomagnesemia); significant bradycardia; family history of sudden cardiac death (see 7 WARNINGS AND PRECAUTIONS, Cardiovascular)
• With concomitant use of other QT/QTc-prolonging drugs (see 7 WARNINGS AND PRECAUTIONS, Cardiovascular; 9.4 Drug-Drug Interactions)

• With concomitant use of CYP3A4/5 inhibitors (See 7 WARNINGS AND PRECAUTIONS,

  • ardiovascular; 9.4 Drug-Drug Interactions; 9.5 Drug-Food Interactions)
• In asthmatics who have previously experienced a serious anti-histamine induced adverse bronchopulmonary effect.
• In patients with porphyria.
• In early (first trimester) pregnancy.

4 DOSAGE AND ADMINISTRATION

4.1 Dosing Considerations

In order to help mitigate the potential risk of QT interval prolongation, HYDROXYZINE should be used for as short a duration as possible, at the lowest effective dose up to specified maximums (see 2 CONTRAINDICATIONS; 4.2 Recommended Dose and Dosage Adjustment; 7 WARNINGS AND PRECAUTIONS, Cardiovascular; 9.4 Drug-Drug Interactions).

4.2 Recommended Dose and Dosage Adjustment

Adults:

• The maximum total daily dose in adults is 100 mg, given in divided doses.

Children and Adolescents:

• In children and adolescents up to 40 kg in weight, the maximum daily dose is 2 mg /kg /day, given in divided doses. (Therefore, at the maximum weight of 40 kg, the maximum daily dose is 80 mg).
• In children and adolescents over 40 kg, the maximum daily dose is the same as for adults: 100 mg per day, given in divided doses.

Geriatric:

• Use should generally be avoided, but if judged to be an appropriate option in an individual case, the maximum daily dose in geriatric patients is 50 mg, given in divided doses.

Hepatic impairment: The total daily dose should be reduced by 33%. Use in patients with severe liver impairment should be avoided.

Renal impairment: For patients with moderate or severe renal impairment, the total daily dosage should be reduced by 50%.

4.5 Missed dose

If the patient misses a dose, instruct the patient to take the dose as soon as they remember. If it is almost time for the next dose, inform the patient to skip the missed dose and continue the regular dosing schedule.

5 OVERDOSAGE

The most common manifestation of HYDROXYZINE overdosage is hypersedation. Other reported signs and symptoms were convulsions, stupor, nausea and vomiting. QT prolongation and torsade de pointes have been observed with excessive blood concentrations of hydroxyzine in a context of overdose or impaired drug metabolism. As in the management of overdosage with any drug, ingestion of multiple agents may have occurred.

General supportive care, including frequent monitoring of the vital signs and close observation of the patient, is indicated. Electrocardiogram monitoring is recommended in the event of overdosage.

Hypotension, though unlikely, may be controlled with intravenous fluids and vasopressors (such as norepinephrine). Do not use epinephrine as HYDROXYZINE counteracts its pressor action. There is no specific antidote. It is doubtful that hemodialysis would be of any value in the treatment of overdosage with hydroxyzine. However, if other agents have been ingested concomitantly, hemodialysis may be indicated.

6 DOSAGE FORMS, STRENGTHS, COMPOSITION AND PACKAGING

Table 1– Dosage Forms, Strengths, Composition and Packaging

Hydroxyzine capsules 10 mg: Off-white paste in an orange opaque soft gel shell printed “10” in white ink.

Hydroxyzine capsules 25 mg: Off-white to yellow paste in a green opaque soft gel shell printed “25” in white ink.

Hydroxyzine capsules 50 mg: Off-white to light pink paste in a red opaque soft gel shell printed “50” in white ink.

Available in bottles of 100.

7 WARNINGS AND PRECAUTIONS

General

Because of its potential anticholinergic actions, HYDROXYZINE should be used with caution in patients with the following conditions:

• angle-closure glaucoma
• increased intraocular pressure
• urinary retention
• bladder outflow obstruction
• prostatic hyperplasia
• pyloroduodenal obstruction
• stenosing peptic ulcer
• decreased GI motility
• myasthenia gravis
• dementia
• breathing problems (e.g., emphysema, chronic bronchitis)
• hyperthyroidism
• cardiovascular disease
• hypertension

Concomitant use with CNS depressants

The potentiating action of hydroxyzine hydrochloride must be considered when the drug is used in conjunction with central nervous system (CNS) depressants such as narcotics, non-narcotic analgesics, hypnotics, sedatives, psychotherapeutic agents, barbiturates or alcohol. Therefore when central nervous system depressants are administered concomitantly with HYDROXYZINE, their dosage should be reduced (see 9.4 Drug-Drug Interactions).

Cardiovascular

Hydroxyzine has been associated with QT/QTc interval prolongation. Rare events of torsade de pointes, cardiac arrest, and sudden death have been reported with hydroxyzine during postmarket use.

Torsade de pointes is a polymorphic ventricular tachyarrhythmia. Generally, the risk of torsade de pointes increases with the magnitude of QT/QTc prolongation produced by the drug. Torsade de pointes may be asymptomatic or experienced by the patient as dizziness, palpitations, syncope, or seizures. If sustained, torsade de pointes can progress to ventricular fibrillation and sudden cardiac death.

Particular care should be exercised when administering hydroxyzine to patients who are suspected to be at an increased risk of experiencing torsade de pointes during treatment with a QT/QTc-prolonging drug. Risk factors for torsade de pointes in the general population include, but are not limited to, the following:

• female gender;
• age 65 years or older;
• baseline prolongation of the QT/QTc interval;
• presence of genetic variants affecting cardiac ion channels or regulatory proteins, especially congenital long QT syndromes;
• family history of sudden cardiac death at <50 years;
• cardiac disease (e.g., myocardial ischemia or infarction, congestive heart failure, left ventricular hypertrophy, cardiomyopathy, conduction system disease);
• history of arrhythmias (especially ventricular arrhythmias, atrial fibrillation, or recent conversion from atrial fibrillation);
• electrolyte disturbances (e.g., hypokalemia, hypomagnesemia, hypocalcemia) or conditions leading to electrolyte disturbances (e.g., gastrointestinal disease, eating disorders);
• bradycardia (<50 beats per minute);
• acute neurological events (e.g., intracranial or subarachnoid haemorrhage, stroke, intracranial trauma);
• diabetes mellitus;
• autonomic neuropathy

When drugs that prolong the QT/QTc interval are prescribed, healthcare professionals should counsel their patients concerning the nature and implications of the ECG changes, underlying diseases and disorders that are considered to represent risk factors, demonstrated and predicted drug-drug interactions, symptoms suggestive of arrhythmia, risk management strategies, and other information relevant to the use of the drug (see also 2 CONTRAINDICATIONS; 4.1 Dosing Considerations; 9.4 Drug-Drug Interactions; 9.5 Drug-Food Interactions).

Driving and Operating Machinery

Since drowsiness may occur with use of this drug, patients should be cautioned against driving a car or operating dangerous machinery while taking HYDROXYZINE.

Neurologic

HYDROXYZINE should be used with caution in patients with seizure disorders, including epilepsy.

Skin

Acute Generalized Exanthematous Pustulosis: Hydroxyzine may rarely cause acute generalized exanthematous pustulosis (AGEP), a serious skin reaction characterized by fever and numerous small, superficial, non-follicular, sterile pustules, arising within large areas of edematous erythema. Inform patients about the signs of AGEP, and discontinue hydroxyzine at the first appearance of a skin rash, worsening of pre-existing skin reactions which hydroxyzine may be used to treat, or any other sign of hypersensitivity. If signs or symptoms suggest AGEP, use of hydroxyzine should not be resumed and alternative therapy should be considered. Avoid cetirizine or levocetirizine in patients who have experienced AGEP or other hypersensitivity reactions with hydroxyzine, due to the risk of cross-sensitivity.

7.1 Special Populations

7.1.1 Pregnant Women

HYDROXYZINE (hydroxyzine hydrochloride) is contraindicated in early pregnancy (see 2 CONTRAINDICATIONS).

Hydroxyzine hydrochloride, when administered to the pregnant mouse, rat, and rabbit, induced fetal abnormalities in the rat and mouse at doses substantially above the human therapeutic range. Clinical data in human beings are inadequate to establish safety in early pregnancy.

7.1.2 Breast-feeding

It is not known whether this drug is excreted in human milk. Since many drugs are so excreted, hydroxyzine should not be given to nursing mothers.

7.1.3 Pediatrics

Based on the data submitted and reviewed by Health Canada, the safety and efficacy of hydroxyzine in pediatric patients has been established. Therefore, Health Canada has authorized an indication for pediatric use. See 1.1 Pediatrics.

7.1.4 Geriatrics

See 4.2 Recommended Dose and Dosage Adjustment; 7 WARNINGS AND PRECAUTIONS, Cardiovascular.

8 ADVERSE REACTIONS

8.1 Adverse Reaction Overview

Side effects reported with the administration of hydroxyzine are usually mild and transitory in nature.

Gastrointestinal disorders: Dry mouth may be encountered at higher dosages.

Nervous system disorders: Drowsiness

Involuntary motor activity, including rare instances of tremor and convulsions, has been reported, usually with doses considerably higher than those recommended.

8.5 Post-Market Adverse Reactions

In post-marketing experience, the following additional undesirable effects have been reported:

Cardiac disorders: Rare cases of cardiac arrest, cardio-respiratory arrest, electrocardiogram QT prolonged, and torsade de pointes, some fatal, have been reported following the use of hydroxyzine-containing products.

Immune system disorders: allergic reaction

Nervous system disorders: headache

Psychiatric disorders: hallucination

Skin and subcutaneous tissue disorders: pruritus, rash, urticaria

9 DRUG INTERACTIONS

9.1 Serious Drug Interactions

9.3 Drug-Behavioural Interactions

HYDROXYZINE may produce additive CNS depressant effects when co-administered with alcohol (see 7 WARNINGS AND PRECAUTIONS, General, Concomitant Use with CNS Depressants).

9.4 Drug-Drug Interactions

QT/QTc-Prolonging Drugs: The concomitant use of hydroxyzine with another QT/QTc-prolonging drug is contraindicated (see 2 CONTRADICATIONS). Drugs that have been associated with QT/QTc interval prolongation and/or torsade de pointes include, but are not limited to, the examples in the following list. Chemical/pharmacological classes are listed if some, although not necessarily all, class members have been implicated in QT/QTc prolongation and/or torsade de pointes:

• Class IA antiarrhythmics (e.g., quinidine, procainamide, disopyramide);
• Class III antiarrhythmics (e.g., amiodarone, sotalol, ibutilide);
• Class 1C antiarrhythmics (e.g., flecainide, propafenone);
• antipsychotics (e.g., chlorpromazine, pimozide, haloperidol, droperidol, ziprasidone, risperidone, olanzapine);
• antidepressants (e.g., fluoxetine, citalopram, venlafaxine, tricyclic/tetracyclic antidepressants e.g., amitriptyline, imipramine, maprotiline);
• opioids (e.g., methadone);
• macrolide antibiotics and analogues (e.g., erythromycin, clarithromycin, azithromycin, tacrolimus);
• quinolone antibiotics (e.g., moxifloxacin, levofloxacin, ciprofloxacin);
• pentamidine;
• antimalarials (e.g., quinine, chloroquine);
• azole antifungals (e.g., ketoconazole, fluconazole, voriconazole);
• domperidone;
• 5-hydroxytryptamine (5-HT)3 receptor antagonists (e.g.,ondansetron);
• arsenic trioxide
• tyrosine kinase inhibitors (e.g., vandetanib, sunitinib, nilotinib);
• histone deacetylase inhibitors (e.g., vorinostat);
• beta-2 adrenoceptor agonists (e.g., salmeterol, formoterol).

CYP3A4/5 Inhibitors: Hydroxyzine is a substrate for CYP3A4/5. Plasma levels of hydroxyzine can be increased by inhibitors of CYP3A4/5. Prolongation of the QT/QTc interval by hydroxyzine is anticipated to be increased in the presence of CYP3A4/5 inhibitors. Drugs that inhibit CYP3A4/5 include, but are not limited to, certain azole antifungals, macrolide antibiotics, and HIV protease inhibitors. The concomitant use of these drugs with hydroxyzine is contraindicated (see 2 CONTRAINDICATIONS).

Drugs that Cause Electrolyte Depletion: The use of hydroxyzine with drugs that can disrupt electrolyte levels is not recommended. Such drugs include, but are not limited to, the following:

• loop, thiazide, and related diuretics;
• laxatives and enemas;
• amphotericin B;
• high dose corticosteroids

The above lists of potentially interacting drugs are not comprehensive. Current information sources should be consulted for newly approved drugs that prolong the QT/QTc interval, inhibit CYP3A4/5, or cause electrolyte disturbances, as well as for older drugs for which these effects have recently been established.

CNS depressant drugs: HYDROXYZINE may potentiate the effects of other central nervous system depressant drugs (see 7 WARNINGS AND PRECAUTIONS, General, Concomitant Use with CNS Depressants).

9.5 Drug-Food Interactions

CYP3A4 can be inhibited by certain foods, including, but not limited to, grapefruit, grapefruit juice, and grapefruit-containing products, which could lead to increased plasma concentrations of hydroxyzine. Patients should be instructed not to consume these foods during treatment with hydroxyzine because the risk of QT/QTc prolongation may be increased.

9.6 Drug-Herb Interactions

Interactions with herbal products have not been established.

9.7 Drug-Laboratory Test Interactions

Treatment should be stopped for one week before skin testing for allergy is undertaken, and for 96 hours prior to a methacholine test.

10 CLINICAL PHARMACOLOGY

Information is not available.

11 STORAGE, STABILITY AND DISPOSAL

Store at controlled room temperature 15°C to 30°C.

HYDROXYZINE should never be disposed of in household trash. Disposal via a pharmacy take back program is recommended.

Keep out of reach and sight of children.

12 SPECIAL HANDLING INSTRUCTIONS

Not applicable

PART II: SCIENTIFIC INFORMATION

13 PHARMACEUTICAL INFORMATION

Drug Substance

Proper name: Hydroxyzine hydrochloride

Chemical name: Ethanol, 2-[2- [(4-chlorophenyl) phenylmethyl] -1 –piperazinyl] ethoxy], dihydrochloride, (±)

Molecular formula and molecular mass: C₂₁H₂₇CIN₂0₂.2HCl and 447.83 g/mol

Structural formula:

Physicochemical properties: Hydroxyzine hydrochloride is a white powder. Melts at 200°C with decomposition. Very soluble in water, soluble in chloroform, slightly soluble in acetone, practically insoluble in ether.

14 CLINICAL TRIALS

The clinical trial data on which the original indications were authorized is not available.

15 MICROBIOLOGY

No microbiological information is required for this drug product.

16 NON-CLINICAL TOXICOLOGY

The non-clinical toxicology data is not available.

.

17 SUPPORTING PRODUCT MONOGRAPHS

1. 1. ATARAX (Hydroxyzine Hydrochloride Oral Solution, 10 mg / 5 mg), submission control 267154, Product Monograph, Searchlight Pharma Inc. (OCT 11, 2022)