DailyMed Label: ORMALVI

DailyMed Label: ORMALVI

2024

DailyMed Prescription

ORMALVI

Dichlorphenamide

Cycle Pharmaceuticals Ltd.

NDC: 70709-085

NDC: 70709-085

NDC: 70709-085

NDC: 70709-085

NDC: 70709-085

NDC: 70709-085

ORMALVI tablets, USP contain dichlorphenamide, an oral carbonic anhydrase inhibitor. Dichlorphenamide, USP a dichlorinated benzenedisulfonamide, is known chemically as 4, 5–dichloro-1,3-benzenedisulfonamide. Its empirical formula is C 6 H 6 Cl 2 N 2 O 4 S 2 and its structural formula is:  Dichlorphenamide USP is a white or practically white, crystalline powder with a molecular weight of 305.16. It is very slightly soluble in water but soluble in dilute solutions of alkali carbonate and hydroxide.  ORMALVI (dichlorphenamide) tablets, USP are supplied as tablets, for oral administration, each containing 50 mg dichlorphenamide. Inactive ingredients are lactose monohydrate, partially pregelatinized starch and magnesium stearate.  FDA approved dissolution test specifications differ from USP. image description

ORMALVI is indicated for the treatment of primary hyperkalemic periodic paralysis, primary hypokalemic periodic paralysis, and related variants. ORMALVI is an oral carbonic anhydrase inhibitor indicated for the treatment of primary hyperkalemic periodic paralysis, primary hypokalemic periodic paralysis, and related variants ( 1 )

• Initiate dosing at 50 mg by mouth once or twice daily ( 2.1 ) • Titrate up or down dose based on individual response ( 2.1 ) • The minimum recommended dosage is 50 mg daily, and the maximum recommended dosage is 200 mg daily ( 2.1 ) • Evaluate response to ORMALVI after 2 months of treatment ( 2.2 ) Initiate dosing at 50 mg by mouth once or twice daily. The dosage may be increased or decreased based on individual response, at weekly intervals (or sooner in case of adverse reaction).  The minimum recommended total daily dosage is 50 mg, and the maximum recommended total daily dosage is 200 mg. Primary hyperkalemic periodic paralysis, primary hypokalemic periodic paralysis, and related variants are a heterogeneous group of conditions, for which the response to ORMALVI may vary. Therefore, prescribers should evaluate the patient's response to ORMALVI after 2 months of treatment to decide whether ORMALVI should be continued. Baseline and periodic measurements of serum potassium and sodium bicarbonate during ORMALVI treatment is recommended [see Warnings and Precautions ( 5.3 , 5.4 )] .

White to off-white, round shaped, flat faced beveled edged tablet, scored on one side, engraved with ‘ZD’ above the score and ‘50’ below the score, the other side is plain. Tablets: 50 mg ( 3 )

ORMALVI is contraindicated in the following circumstances: Hypersensitivity to dichlorphenamide or other sulfonamides [see Warnings and Precautions ( 5.1 )] Concomitant use of ORMALVI and high dose aspirin [see Warnings and Precautions ( 5.2 ) and Drug Interactions ( 7.1 )] Severe pulmonary disease, limiting compensation to metabolic acidosis caused by ORMALVI  [see Warnings and Precautions ( 5.4 )] Hepatic insufficiency: ORMALVI may aggravate hepatic encephalopathy. Hepatic insufficiency ( 4 ) Severe pulmonary obstruction ( 4 ) Hypersensitivity to dichlorphenamide or other sulfonamides ( 4 ) Concomitant use with high dose aspirin ( 4 )

Hypersensitivity and Other Life-Threatening Reactions: discontinue ORMALVI at the first appearance of skin rash or any sign of immune-mediated or idiosyncratic adverse reaction ( 5.1 ) Hypokalemia: baseline and periodic measurements of serum potassium are recommended; if hypokalemia develops or persists, consider reducing the dose or discontinuing ORMALVI and correcting potassium levels ( 5.3 ) Metabolic acidosis: baseline and periodic measurements of serum bicarbonate are recommended; if metabolic acidosis develops or persists, consider reducing the dose or discontinuing ORMALVI ( 5.4 ) Falls: consider reducing the dose or discontinuing ORMALVI in patients who experience falls ( 5.5 ) Fatalities associated with the administration of sulfonamides have occurred because of adverse reactions including Stevens-Johnson syndrome, toxic epidermal necrolysis, fulminant hepatic necrosis, agranulocytosis, aplastic anemia, and other blood dyscrasias. Pulmonary involvement can occur in isolation or as part of a systemic reaction. ORMALVI should be discontinued at the first appearance of skin rash or any sign of immune-mediated or other life-threatening adverse reaction. Carbonic anhydrase inhibitors, including ORMALVI, can cause metabolic acidosis [see Warnings and Precautions ( 5.4 )] , which can increase the risk of salicylate toxicity. Anorexia, tachypnea, lethargy, and coma have been reported with concomitant use of dichlorphenamide and high-dose aspirin. Therefore, the concomitant use of ORMALVI and high-dose aspirin is contraindicated.  Patients with concomitant use of  ORMALVI and low-dose aspirin should be carefully monitored. ORMALVI increases potassium excretion and can cause hypokalemia. The risk of hypokalemia is greater when ORMALVI is used in patients with conditions associated with hypokalemia (e.g., adrenocortical excess, renal tubular acidosis type 1 and 2), and in patients receiving other drugs that may cause hypokalemia [see Drug Interactions ( 7.3 )]. Baseline and periodic measurements of serum potassium during ORMALVI treatment is recommended. If hypokalemia develops or persists, consideration should be given to reducing the dose or discontinuing ORMALVI and correction of potassium levels. ORMALVI can cause hyperchloremic non-anion gap metabolic acidosis. Concomitant use of ORMALVI with other drugs that cause metabolic acidosis may increase the severity of acidosis. Concomitant use of ORMALVI in compensated patients with respiratory acidosis, such as in advanced lung diseases, may lead to respiratory decompensation. Baseline and periodic measurements of serum bicarbonate during ORMALVI treatment are recommended. If metabolic acidosis develops or persists, consideration should be given to reducing the dose or discontinuing ORMALVI  [see Drug Interactions ( 7.4) ]. ORMALVI increases the risk of falls. The risk of falls is greater in the elderly and with higher doses of ORMALVI. Consider dose reduction or discontinuation of ORMALVI in patients who experience falls while treated with ORMALVI.

The following serious adverse reactions are described elsewhere in labeling:

Aspirin: anorexia, tachypnea, lethargy, and coma have been reported with concomitant use of dichlorphenamide and high-dose aspirin. The concomitant use of ORMALVI and high-dose aspirin is contraindicated. ORMALVI should be used with caution in patients receiving lower doses of aspirin ( 4 , 5.2 , 7.1 ) Carbonic anhydrase inhibitors, including ORMALVI, can cause metabolic acidosis [see Warning and Precautions ( 5.2 , 5.4 )] , which can increase the risk of salicylate toxicity. Anorexia, tachypnea, lethargy, and coma have been reported with concomitant use of dichlorphenamide and high-dose aspirin. Therefore, concomitant use of ORMALVI and high-dose aspirin is contraindicated. Patients with concomitant use of ORMALVI and low-dose aspirin should be carefully monitored [see Contraindications ( 4 ) and Warnings and Precautions ( 5.2 )]. In vitro , dichlorphenamide is an inhibitor of OAT1 transporters. The concomitant administration of ORMALVI may increase the plasma exposures of OAT1 substrates. Use of ORMALVI with drugs that are sensitive to OAT1 inhibition (e.g., methotrexate, famotidine, oseltamivir) is not recommended [see Clinical Pharmacology ( 12.3 )]. The risk of hypokalemia is greater with coadministration of ORMALVI and other drugs that can cause hypokalemia (e.g., loop diuretics, thiazide diuretics, laxatives, antifungals, penicillins, and theophylline) [see Warnings and Precautions ( 5.3 )]. Coadministration of ORMALVI and other drugs that can cause metabolic acidosis may increase the severity of the acidosis [see Warnings and Precautions ( 5.4 )]. An in vitro transporter study indicated that dichlorphenamide is a substrate of human transporters OAT1 and OAT3 [see Clinical Pharmacology ( 12.3 )] . Therefore, signs of dichlorphenamide toxicity should be monitored when administered with OAT1 or OAT3 inhibitors.

Pregnancy: Based on animal data, may cause fetal harm ( 8.1 ) Risk Summary There are no adequate data on the developmental risk associated with the use of ORMALVI in pregnant women. A no-effect dose has not been established. Dichlorphenamide was teratogenic when administered orally to pregnant rats. The background risk of major birth defects and miscarriage for the indicated population is unknown. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4%, and 15% to 20%, respectively. Clinical Considerations Fetal/Neonatal adverse reactions ORMALVI treatment can cause metabolic acidosis [see Warnings and Precautions ( 5.4 )] . The effect of dichlorphenamide-induced metabolic acidosis has not been studied in pregnancy; however, metabolic acidosis in pregnancy (due to other causes) can cause decreased fetal growth, decreased fetal oxygenation, and fetal death, and may affect the fetus’ ability to tolerate labor. Pregnant patients should be monitored for metabolic acidosis and treated as in the nonpregnant state. Newborns of mothers treated with ORMALVI should be monitored for metabolic acidosis because of possible occurrence of transient metabolic acidosis following birth. Labor or Delivery Although the effect of ORMALVI on labor and delivery in humans has not been established, the development of dichlorphenamide-induced metabolic acidosis in the mother and/or in the fetus might affect the fetus’ ability to tolerate labor. Data Animal Data Teratogenic effects (fetal limb reduction defects) were reported following oral administration of dichlorphenamide to pregnant rats during organogenesis at 350 mg/kg, or 17 times the maximum recommended human dose (200 mg/day) on a body surface area (mg/m 2 ) basis. A no-effect dose for adverse effects on embryofetal development has not been established. Risk Summary There are no data on the presence of dichlorphenamide in human milk, the effects on the breastfed infant, or the effects on milk production. The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for ORMALVI and any potential adverse effects on the breastfed infant from ORMALVI or from the underlying maternal condition. Safety and effectiveness of ORMALVI in pediatric patients have not been established. The risk of falls and of metabolic acidosis are greater in elderly patients [see Warnings and Precautions ( 5.4 , 5.5 )].

Each ORMALVI (dichlorphenamide) tablet USP, 50 mg is white to off-white, round shaped, flat faced beveled edged tablet, scored on one side, engraved with ‘ZD’ above the score and ‘50’ below the score, the other side is plain. ORMALVI (dichlorphenamide) tablets are supplied as follows: Bottles of 100                                       NDC 70709-085-10 Store at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) [See USP Controlled Room Temperature].

Dichlorphenamide is a carbonic anhydrase inhibitor. However, the precise mechanism by which dichlorphenamide exerts its therapeutic effects in patients with primary periodic paralysis is unknown. ORMALVI can cause metabolic acidosis, which can increase the risk of salicylate toxicity with coadministration [see Warnings and Precautions ( 5.2 )] . ORMALVI-induced metabolic acidosis can also increase in severity with coadministration of other drugs that cause metabolic acidosis [see Warnings and Precautions ( 5.4 )]. After single-dose administration in healthy subjects in fasted state, dichlorphenamide C max and AUC increased in a dose-proportional manner within the range of 25 mg to 400 mg (2 times the maximum recommended dose). The steady-state is expected to be achieved within 10 days of twice-daily dosing. Absorption The median time to reach maximum concentration (T max ) of dichlorphenamide was about 1.5 to 3 hours postdose after both single and multiple dose administrations. Distribution The plasma protein binding of dichlorphenamide is approximately 88%. Elimination Following a single-dose administration, mean terminal half-life was in the range of 32 to 66 hours. Metabolism Dichlorphenamide is not a substrate for CYP1A2, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6 and CYP3A4 isoforms when tested in vitro . Drug Interaction Studies In vitro Assessment of Drug Interactions Drug-Metabolizing Enzyme Inhibition Dichlorphenamide is not an inhibitor for CYP1A2, 2B6, 2C8, 2C9, 2C19, 2D6, or 3A4 enzymes when tested in vitro. Drug-Metabolizing Enzyme Induction Dichlorphenamide is not an inducer for CYP1A2, 2B6, or 3A4 enzymes when tested in vitro . In vitro Assessment of Transporter-Drug Interactions Dichlorphenamide is neither a substrate nor inhibitor for p-gp, BCRP, OATP1B1, OATP1B3, OAT2, OAT4, OCT1, OCT2, MATE1, or MATE2-K when tested in vitro . Dichlorphenamide is not an inhibitor of OAT3, but is an inhibitor of OAT1 based on in vitro studies [see Drug Interactions ( 7.4 )]. Dichlorphenamide is a substrate for transporters OAT1 and OAT3 based on in vitro studies [see Drug Interactions ( 7.2 )].  In Vivo Drug Interactions The use of dichlorphenamide in combination with high-dose aspirin is contraindicated as it may lead to salicylate toxicity. The mechanism(s) of this interaction is not known. Specific Populations Geriatrics The pharmacokinetics of dichlorphenamide in the elderly has not been determined.

Carcinogenesis Studies to assess the carcinogenic potential of dichlorphenamide have not been conducted. Mutagenesis Studies to assess the genotoxicity of dichlorphenamide have not been conducted. Impairment of Fertility Studies to assess the effects of dichlorphenamide on fertility have not been conducted.

The efficacy of ORMALVI was evaluated in two clinical studies, Study 1 and Study 2. Study 1 Study 1 was a 9-week, double-blind, placebo-controlled multi-center study. Study 1 consisted of two substudies: a substudy in patients with hypokalemic periodic paralysis (n=44), and a substudy in patients with hyperkalemic periodic paralysis (n=21). The primary efficacy endpoint in both substudies was the average number of self-reported attacks of muscle weakness per week over the final 8 weeks of the trial. Withdrawal from the study for acute severe worsening (increase in attack frequency or severity) was also assessed as an endpoint. In Study 1, the dose of ORMALVI was 50 mg b.i.d. for treatment-naïve patients. Patients already on dichlorphenamide prior to the study continued on the same dose while on ORMALVI during the study. In patients taking acetazolamide prior to the study, the dose of ORMALVI was set at 20% of the acetazolamide dose. Dose reduction for tolerability was permitted. Hypokalemic Periodic Paralysis Substudy of Study 1 In the hypokalemic periodic paralysis substudy, median age of patients was 45 years and 73% of patients were male. Patients treated with ORMALVI (n=24) had 2.2 fewer attacks per week than patients (n=20) treated with placebo (p=0.02). None of the patients randomized to ORMALVI reached the endpoint of withdrawal from the study for acute worsening, vs. five patients randomized to placebo. The mean dose of ORMALVI at Week 9 was 94 mg/day. Hyperkalemic Periodic Paralysis Substudy of Study 1 In the Hyperkalemic Periodic Paralysis substudy, median age of patients was 43 years and 43% of patients were male. During the double-blind treatment period, patients treated with ORMALVI (n=12) had 3.9 fewer attacks per week than patients (n=9) treated with placebo (p=0.08). None of the patients randomized to ORMALVI reached the endpoint of withdrawal from the study for acute worsening, vs. two patients randomized to placebo. The mean dose of ORMALVI at Week 9 was 82 mg/day. Study 2 Study 2 was a 35-week, double-blind, placebo-controlled, multi-center, two-period crossover study. Study 2 also consisted of two substudies: a substudy in patients with hypokalemic periodic paralysis (n=42), and a substudy in patients with hyperkalemic periodic paralysis (n=31), including patients with Paramyotonia Congenita. The primary endpoint in the hypokalemic periodic paralysis substudy was the incidence of acute intolerable worsening (based on attack frequency or severity) necessitating withdrawal. The primary endpoint in the hyperkalemic periodic paralysis substudy was the average number of self-reported attacks of muscle weakness per week. Dosing was determined similarly to Study 1. Hypokalemic Periodic Paralysis Substudy of Study 2 The hypokalemic periodic paralysis substudy included patients with a mean age of 38 years; 79% of patients were male. Acute intolerable worsening was observed in 2 patients on ORMALVI vs. 11 patients on placebo (p=0.02). The mean dose of ORMALVI at the end of the study was 96 mg/day. Hyperkalemic Periodic Paralysis Substudy of Study 2 The hyperkalemic periodic paralysis substudy included patients with a mean age of 37 years; and 79% of patients were male. Patients treated had 2.3 fewer attacks per week on ORMALVI than on placebo (p=0.006). The mean dose of ORMALVI at the end of the study was 73 mg/day.

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