Propayerst Plus

Hydrochlorothiazide:

• Propayerst Plus information
• Propayerst Plus indications
• Propayerst Plus warnings
• Propayerst Plus intake guidelines
• Propayerst Plus dosage
• Propayerst Plus overdose
• Propayerst Plus missed dose
• Propayerst Plus side effects
• Propayerst Plus drug reactions
• Propayerst Plus (Hydrochlorothiazide) reviews

Propayerst Plus information

Propayerst Plus (Hydrochlorothiazide) is an antihypertensive, diuretic drug that acts on the electrolyte reabsorption in the renal tubular mechanism increasing the excretion of chloride and sodium in equivalent amounts. The exact mechanism of its antihypertensive action is not known at this time.

Propayerst Plus indications

Propayerst Plus (Hydrochlorothiazide) is typically employed for the treatment of patients suffering from hypertension, either as monotherapy or in combination with other antihypertensive medication. It is also employed in some cases as a diuretic agent. Propayerst Plus (Hydrochlorothiazide) therapy may also be prescribed for the treatment of hepatic cirrhosis, edema (in patients suffering from congestive heart failure), nephrotic syndrome, drug induced edema, chronic renal failure or acute glomerulonephritis. Health care professionals may prescribe this drug in order to treat other medical conditions as well; if you would like to know more about the reasons you have been prescribed this drug, it is advised to ask your personal physician.

Propayerst Plus warnings

Propayerst Plus (Hydrochlorothiazide) may not be used in the treatment of patients who are allergic to this drug, any of its components or other sulfonamide-derived medication. Also, this drug may not be suitable for use in patients that are suffering from anuria, azotemia or impaired renal functions. Caution should be employed if the patient is suffering from hepatic disease. Other medical conditions may also influence the examining health care provider's decision of prescribing Propayerst Plus (Hydrochlorothiazide); it is strongly recommended to make sure that the health care professional is fully aware of your health condition and medical history before starting a treatment with this drug.

Use of Propayerst Plus (Hydrochlorothiazide) during pregnancy or breast-feeding is also not recommended. This medicine may affect an unborn baby and it also passes into breast milk. As such, use of this drug in pregnant women or breast-feeding mothers should not be employed.

Propayerst Plus intake guidelines

You should always take Propayerst Plus (Hydrochlorothiazide) as you have been directed by the prescribing health care specialist. While in some cases daily administration of the drug is recommended, other patients may be prescribed an intermittent therapy. Also, the number of daily doses may vary. As such, it is best that you do not follow another patient's intake schedule. If you have difficulties understanding the intake guidelines that your prescribing health care professional has provided, you should ask for further explanations from an authorized health care specialist - such as a pharmacist, a doctor or a nurse.

Propayerst Plus dosage

The exact Propayerst Plus (Hydrochlorothiazide) dosage may vary greatly from one case to another, depending on the condition being treated, on the patient's medical history and general health condition, on his or her age as well as on a number of other factors. As such you are advised to use the exact Propayerst Plus (Hydrochlorothiazide) dosage that has been prescribed to you and never use the dosage prescribed to another patient or a dosage that you have been prescribed in the past. Taking a different Propayerst Plus (Hydrochlorothiazide) dose may cause the treatment to not have the desired effect, and if you take this drug in larger doses you may have a higher risk of developing side effects, or you may suffer from an overdose.

Propayerst Plus overdose

You should never exceed the Propayerst Plus (Hydrochlorothiazide) prescribed dosage, in order to avoid an overdose with this medication. However, if you consider that you are affected by an overdose with this drug it is advised to immediately consult your personal health care provider, the local poisons center or to go to the nearest medical facility to seek emergency medical attention. The common symptoms of an overdose with Propayerst Plus (Hydrochlorothiazide) are dehydration and cardiac arrhythmia. The patient may also suffer from electrolyte depletion and thus may present the relevant signs and symptoms.

Propayerst Plus missed dose

In case you have missed a dose of Propayerst Plus (Hydrochlorothiazide), it is advised that you take the dose as soon as you remember. If the moment when you remember is too close to another intake of the medication, you should completely skip the missed Propayerst Plus (Hydrochlorothiazide) dose and take the next scheduled dose on time. You should never take a larger dose of the drug in order to make up for a missed dose, unless your prescribing health care provider directs you to do so.

Propayerst Plus side effects

In some patients Propayerst Plus (Hydrochlorothiazide) may cause side effects. While they are not very common, it is recommended to let your personal health care provider know if you begin experiencing any side effects. Several types of symptoms are possible: dizziness, headache, paresthesias, gastric irritation, anorexia, nausea and vomiting, diarrhea or constipation, pancreatitis, jaundice, hypotension. Metabolic side effects may include glycosuria, hyperglycemia, hyperuricemia, hypokalemia or hyponatremia. Renal failure or dysfunction may develop, as well as interstitial nephritis. Some patients reported experiencing muscle spasms, restlessness, unusual weakness and blurred vision. In some cases photosensitivity, anaphylactic reactions, respiratory distress, fever, rashes, vasculitis or toxic epidermal necrolysis have occurred.

Propayerst Plus drug reactions

Propayerst Plus (Hydrochlorothiazide) may interact with barbiturates and narcotics, as well as with alcohol. If you are also following a treatment course with antidiabetic drugs, their dosage may need to be adjusted before starting to take Propayerst Plus (Hydrochlorothiazide). This drug may have an additive effect with other antihypertensive medication. ACE inhibitors, ACTH, corticosteroids and skeletal muscle relaxants may also interact with this drug causing unwanted effects. This drug may not be properly absorbed if the patient is also taking Colestipol resins or Cholestyramine. NSAIDs, lithium and Pressor amines may affect or be affected by Propayerst Plus (Hydrochlorothiazide), and as such it is strongly recommended to let the prescribing health care provider know if you are taking these or any other drugs before starting a therapy course with this medicine. Other drug interactions that are not listed here are also possible.

Propranolol Hydrochloride:

• Description
• Clinical pharmacology
• Clinical studies
• Indications & usage
• Contraindications
• Warnings
• Precautions
• Adverse reactions
• Overdosage
• Dosage & administration
• How supplied
• Propayerst Plus (Propranolol Hydrochloride) reviews

DESCRIPTION

Propayerst Plus (Propranolol Hydrochloride) Hydrochloride, USP is a synthetic beta-adrenergic receptor blocking agent chemically described as (+)-1-(isopropylamino)-3-(1-naphthyloxy)-2-propanol hydrochloride. Its structural formula is:

Propayerst Plus (Propranolol Hydrochloride) Hydrochloride, USP is a stable, white, crystalline solid which is readily soluble in water and ethanol. Its molecular weight is 295.80.

Propayerst Plus (Propranolol Hydrochloride) Hydrochloride Injection, USP is available as a sterile injectable solution for intravenous administration. Each mL contains 1 mg of Propayerst Plus (Propranolol Hydrochloride) Hydrochloride, USP in Water for Injection, USP. The pH is adjusted with anhydrous Citric Acid, USP.

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CLINICAL PHARMACOLOGY

General

Propayerst Plus (Propranolol Hydrochloride) is a nonselective beta-adrenergic receptor blocking agent possessing no other autonomic nervous system activity. It specifically competes with beta-adrenergic receptor stimulating agents for available receptor sites. When access to beta-recceptor sites is blocked by Propayerst Plus (Propranolol Hydrochloride), chronotropic, inotropic, and vasodilator responses to beta-adrenergic stimulation are decreased proportionately. At doses greater than required for beta blockade, Propayerst Plus (Propranolol Hydrochloride) also exerts a quinidine-like or anesthetic-like membrane action, which affects the cardiac action potential. The significance of the membrane action in the treatment of arrhythmias is uncertain.

Mechanism of Action

The effects of Propayerst Plus (Propranolol Hydrochloride) are due to selective blockade of beta-adrenergic receptors, leaving alpha-adrenergic responses intact. There are two well-characterized subtypes of beta receptors (beta_1 and beta_2); Propayerst Plus (Propranolol Hydrochloride) interacts with both subtypes equally. Beta_1-adrenergic receptors leads to a decrease in the activity of both normal and ectopic pacemaker cells and a decrease in A-V nodal conduction velocity. All of these actions can contribute to antiarrhythmic activity and control of ventricular rate during arrhythmias. Blockade of cardiac beta_1-adrenergic receptors also decreases the myocardial force of contraction and may provoke cardiac decompensation in patients with minimal cardiac reserve.

Beta_2-adrenergic receptors are found predominantly in smooth muscle-vascular, bronchial, gastrointestinal and genitourinary. Blockade of these receptors results in constriction. Clinically, Propayerst Plus (Propranolol Hydrochloride) may exacerbate respiratory symptoms in patients with obstructive pulmonary diseases such as asthma and emphysema.

Propranolol's beta blocking effects are attributable to its S(-) enantiomer.

Pharmacokinetics and Drug Metabolism

Distribution

Propayerst Plus (Propranolol Hydrochloride) has a distribution half-life (T1/2 alpha) of 5-10 minutes and a volume of distribution of about 4 to 5 L/kg. Approximately 90% of circulating Propayerst Plus (Propranolol Hydrochloride) is bound to plasma proteins. The binding is enantiomer-selective. The S-isomer is preferentially bound to alpha_1 glycoprotein and the R-isomer is preferentially bound to albumin.

Metabolism and Elimination

The elimination half-life (T½ beta) is between 2 and 5.5 hours. Propayerst Plus (Propranolol Hydrochloride) is extensively metabolized with most metabolites appearing in the urine. The major metabolites include Propayerst Plus (Propranolol Hydrochloride) glucuronide, naphthyloxylactic acid, and glucuronic acid and sulfate conjugates of 4-hydroxy Propayerst Plus (Propranolol Hydrochloride). Following single-dose intravenous administration, side-chain oxidative products account for approximately 40% of the metabolites, direct conjugation products account for approximately 45-50% of metabolites, and ring oxidative products account for approximately 10-15% of metabolites. Of these, only the primary ring oxidative product (4-hydroxypropranolol) possesses beta-adrenergic receptor blocking activity.

In vitro studies have indicated that the aromatic hydroxylation of Propayerst Plus (Propranolol Hydrochloride) is catalyzed mainly by polymorphic CYP2D6. Side‑chain oxidation is mediated mainly by CYP1A2 and to some extent by CYP2D6. 4-hydroxy Propayerst Plus (Propranolol Hydrochloride) is a weak inhibitor of CYP2D6.

Pharmacodynamics

As Propayerst Plus (Propranolol Hydrochloride) concentration increases, so does its beta-blocking effect, as evidenced by a reduction in exercise-induced tachycardia (n = 6 normal volunteers).

Special Populations

Pediatric

The pharmacokinetics of Propayerst Plus (Propranolol Hydrochloride) have not been investigated in patients under 18 years of age. Propayerst Plus (Propranolol Hydrochloride) injection is not recommended for treatment of cardiac arrhythmias in pediatric patients.

Geriatric

Elevated Propayerst Plus (Propranolol Hydrochloride) plasma concentrations, a longer mean elimination half-life (254 vs. 152 minutes), and decreased systemic clearance (8 vs. 13 mL/kg/min) have been observed in elderly subjects when compared to young subjects. However, the apparent volume of distribution seems to be similar in elderly and young subjects. These findings suggest that dose adjustment of Propayerst Plus (Propranolol Hydrochloride) injection may be required for elderly patients.

Gender

Intravenously administered Propayerst Plus (Propranolol Hydrochloride) was evaluated in 5 women and 6 men. When adjusted for weight, there were no gender-related differences in elimination half-life, volume of distribution, protein binding, or systemic clearance.

Obesity

In a study of intravenously administered Propayerst Plus (Propranolol Hydrochloride), obese subjects had a higher AUC (161 versus 109 hr·mcg/L) and lower total clearance than did non-obese subjects. Propayerst Plus (Propranolol Hydrochloride) plasma protein binding was similar in both groups.

Renal Insufficiency

The pharmacokinetics of Propayerst Plus (Propranolol Hydrochloride) and its metabolites were evaluated in 15 subjects with varying degrees of renal function after Propayerst Plus (Propranolol Hydrochloride) administration via the intravenous and oral routes. When compared with normal subjects, an increase in fecal excretion of Propayerst Plus (Propranolol Hydrochloride) conjugates was observed in patients with increased renal impairment. Propayerst Plus (Propranolol Hydrochloride) was also evaluated in 5 patients with chronic renal failure, 6 patients on regular dialysis, and 5 healthy subjects, following a single oral dose of 40 mg of Propayerst Plus (Propranolol Hydrochloride). The peak plasma concentrations (Cmax) of Propayerst Plus (Propranolol Hydrochloride) in the chronic renal failure group were 2- to 3-fold higher (161 ng/mL) than those observed in the dialysis patients (47 ng/‌mL) and in the healthy subjects (26 ng/mL). Propayerst Plus (Propranolol Hydrochloride) plasma clearance was also reduced in the patients with chronic renal failure.

Chronic renal failure has been associated with a decrease in drug metabolism via downregulation of hepatic cytochrome P-450 activity.

Hepatic Insufficiency

Propayerst Plus (Propranolol Hydrochloride) is extensively metabolized by the liver. In a study conducted in 6 normal subjects and 20 patients with chronic liver disease, including hepatic cirrhosis, 40 mg of R-propranolol was administered intravenously. Compared to normal subjects, patients with chronic liver disease had decreased clearance of Propayerst Plus (Propranolol Hydrochloride), increased volume of distribution, decreased protein-binding, and considerable variation in half-life. Caution should be exercised when Propayerst Plus (Propranolol Hydrochloride) is used in this population. Consideration should be given to lowering the dose of intravenous Propayerst Plus (Propranolol Hydrochloride) in patients with hepatic insufficiency.

Thyroid Dysfunction

No pharmacokinetic changes were observed in hyperthyroid or hypothyroid patients when compared to their corresponding euthyroid state. Dosage adjustment does not seem necessary in either patient population based on pharmacokinetic findings.

Drug Interactions

Interactions with Substrates, Inhibitors or Inducers of Cytochrome P-450 Enzymes

Because propranolol’s metabolism involves multiple pathways in the cytochrome P-450 system (CYP2D6, 1A2, 2C19), administration of Propayerst Plus (Propranolol Hydrochloride) with drugs that are metabolized by, or affect the activity (induction or inhibition) of one or more of these pathways may lead to clinically relevant drug interactions.

Substrates or Inhibitors of CYP2D6

Blood levels of Propayerst Plus (Propranolol Hydrochloride) may be increased by administration of Propayerst Plus (Propranolol Hydrochloride) with substrates or inhibitors of CYP2D6, such as amiodarone, cimetidine, delavirdine, fluoxetine, paroxetine, quinidine, and ritonavir. No interactions were observed with either ranitidine or lansoprazole.

Substrates or Inhibitors of CYP1A2

Blood levels of Propayerst Plus (Propranolol Hydrochloride) may be increased by administration of Propayerst Plus (Propranolol Hydrochloride) with substrates or inhibitors of CYP1A2, such as imipramine, cimetidine, ciprofloxacin, fluvoxamine, isoniazid, ritonavir, theophylline, zileuton, zolmitriptan, and rizatriptan.

Substrates or Inhibitors of CYP2C19

Blood levels of Propayerst Plus (Propranolol Hydrochloride) may be increased by administration of Propayerst Plus (Propranolol Hydrochloride) with substrates or inhibitors of CYP2C19, such as fluconazole, cimetidine, fluoxetine, fluvoxamine, teniposide, and tolbutamide. No interaction was observed with omeprazole.

Inducers of Hepatic Drug Metabolism

Blood levels of Propayerst Plus (Propranolol Hydrochloride) may be decreased by administration of Propayerst Plus (Propranolol Hydrochloride) with inducers such as rifampin and ethanol. Cigarette smoking also induces hepatic metabolism and has been shown to increase up to 100% the clearance of Propayerst Plus (Propranolol Hydrochloride), resulting in decreased plasma concentrations.

Cardiovascular Drugs

Antiarrhythmics

The AUC of propafenone is increased by more than 200% with co-administration of Propayerst Plus (Propranolol Hydrochloride).

The metabolism of Propayerst Plus (Propranolol Hydrochloride) is reduced by co-administration of quinidine, leading to a 2- to 3-fold increased blood concentrations and greater beta-blockade.

The metabolism of lidocaine is inhibited by co-administration of Propayerst Plus (Propranolol Hydrochloride), resulting in a 25% increase in lidocaine concentrations.

Calcium Channel Blockers

The mean Cmax and AUC of Propayerst Plus (Propranolol Hydrochloride) are increased respectively, by 50% and 30% by co-administration of nisoldipine and by 80% and 47%, by co-administration of nicardipine.

The mean values of Cmax and AUC of nifedipine are increased by 64% and 79%, respectively, by co-administration of Propayerst Plus (Propranolol Hydrochloride).

Propayerst Plus (Propranolol Hydrochloride) does not affect the pharmacokinetics of verapamil and norverapamil. Verapamil does not affect the pharmacokinetics of Propayerst Plus (Propranolol Hydrochloride).

Non-Cardiovascular Drugs

Migraine Drugs

Administration of zolmitriptan or rizatriptan with Propayerst Plus (Propranolol Hydrochloride) resulted in increased concentrations of zolmitriptan (AUC increased by 56% and Cmax by 37%) or rizatriptan (the AUC and Cmax were increased by 67% and 75%, respectively).

Theophylline

Co-administration of theophylline with Propayerst Plus (Propranolol Hydrochloride) decreases theophylline clearance by 33% to 52%.

Benzodiazepines

Propayerst Plus (Propranolol Hydrochloride) can inhibit the metabolism of diazepam, resulting in increased concentrations of diazepam and its metabolites. Diazepam does not alter the pharmacokinetics of Propayerst Plus (Propranolol Hydrochloride).

The pharmacokinetics of oxazepam, triazolam, lorazepam, and alprazolam are not affected by co-administration of Propayerst Plus (Propranolol Hydrochloride).

Neuroleptic Drugs

Co-administration of Propayerst Plus (Propranolol Hydrochloride) at doses greater than or equal to 160 mg/day resulted in increased thioridazine plasma concentrations ranging from 50% to 370% and increased thioridazine metabolites concentrations ranging from 33% to 210%.

Co-administration of chlorpromazine with Propayerst Plus (Propranolol Hydrochloride) resulted in increased plasma levels of both drugs (70% increase in Propayerst Plus (Propranolol Hydrochloride) concentrations).

Anti-Ulcer Drugs

Co-administration of Propayerst Plus (Propranolol Hydrochloride) with cimetidine, a non-specific CYP450 inhibitor, increased Propayerst Plus (Propranolol Hydrochloride) concentrations by about 40%. Co‑administration with aluminum hydroxide gel (1200 mg) resulted in a 50% decrease in Propayerst Plus (Propranolol Hydrochloride) concentrations.

Co-administration of metoclopramide with Propayerst Plus (Propranolol Hydrochloride) did not have a significant effect on propranolol’s pharmacokinetics.

Lipid Lowering Drugs

Co-administration of cholesteramine or colestipol with Propayerst Plus (Propranolol Hydrochloride) resulted in up to 50% decrease in Propayerst Plus (Propranolol Hydrochloride) concentrations.

Co-administration of Propayerst Plus (Propranolol Hydrochloride) with lovastatin or pravastatin decreased 20% to 25% the AUC of both, but did not alter their pharmacodynamics. Propayerst Plus (Propranolol Hydrochloride) did not have an effect on the pharmacokinetics of fluvastatin.

Warfarin

Concomitant administration of Propayerst Plus (Propranolol Hydrochloride) and warfarin has been shown to increase warfarin bioavailability and increase prothrombin time.

CLINICAL STUDIES

In a series of 225 patients with supraventricular (n = 145), ventricular (n = 69), or both (n = 11) arrythmias resistant to digitalis, intravenous Propayerst Plus (Propranolol Hydrochloride) hydrochloride was administered in single doses, averaging 1 to 5 mg. Approximately one-quarter of the patients with supraventricular arrhythmias (generally those with sinus or atrial tachycardia) reverted to normal sinus rhythm. About one-half had symptoms ameliorated either by a decrease in ventricular rate or an attenuation of frequency or severity of paroxysmal attacks.

Approximately one-half of patients with ventricular arrhythmias (generally those with frequent PVCs) reverted to normal sinus rhythm or responded with a reduction in ventricular rate.

Similar findings were seen in a series of 25 Bantu patients with atrial fibrillation (n = 16), sinus tachycardia (n = 5), and multifocal ventricular extrasystoles (n = 9).

In another series, 7 of 8 patients with digitalis-related tachyarrhythmia had ventricular rate decreases after intravenous Propayerst Plus (Propranolol Hydrochloride). Similarly limited clinical experience has shown that intravenous Propayerst Plus (Propranolol Hydrochloride) will slow the ventricular rate in patients with Wolff-Parkinson-White syndrome or with tachycardia associated with thyrotoxicosis.

Onset of activity is usually within five minutes.

INDICATIONS & USAGE

Cardiac Arrhythmias

Intravenous administration is usually reserved for life-threatening arrhythmias or those occurring under anesthesia.

1. Supraventricular arrhythmias

Intravenous Propayerst Plus (Propranolol Hydrochloride) is indicated for the short-term treatment of supraventricular tachycardia, including Wolff‑Parkinson‑White syndrome and thyrotoxicosis, to decrease ventricular rate. Use in patients with atrial flutter or atrial fibrillation should be reserved for arrythmias unresponsive to standard therapy or when more prolonged control is required. Reversion to normal sinus rhythm has occasionally been observed, predominantly in patients with sinus or atrial tachycardia.

2. Ventricular tachycardias

With the exception of those induced by catecholamines or digitalis, Propayerst Plus (Propranolol Hydrochloride) is not the drug of first choice. In critical situations when cardioversion techniques or other drugs are not indicated or are not effective, Propayerst Plus (Propranolol Hydrochloride) may be considered. If, after consideration of the risks involved, Propayerst Plus (Propranolol Hydrochloride) is used, it should be given intravenously in low dosage and very slowly, as the failing heart requires some sympathetic drive for maintenance of myocardial tone. Some patients may respond with complete reversion to normal sinus rhythm, but reduction in ventricular rate is more likely. Ventricular arrhythmias do not respond to Propayerst Plus (Propranolol Hydrochloride) as predictably as do the supraventricular arrhythmias.

Intravenous Propayerst Plus (Propranolol Hydrochloride) is indicated for the treatment of persistent premature ventricular extrasystoles that impair the well‑being of the patient and do not respond to conventional measures.

3. Tachyarrhythmias of digitalis intoxication

Intravenous Propayerst Plus (Propranolol Hydrochloride) is indicated to control ventricular rate in life-threatening digitalis-induced arrhythmias. Severe bradycardia may occur.

4. Resistant tachyarrhythmias due to excessive catecholamine action during anesthesia

Intravenous Propayerst Plus (Propranolol Hydrochloride) is indicated to abolish tachyarrhythmias due to excessive catecholamine action during anesthesia when other measures fail. These arrhythmias may arise because of release of endogenous catecholamines or administration of catecholamines. All general inhalation anesthetics produce some degree of myocardial depression. Therefore, when Propayerst Plus (Propranolol Hydrochloride) is used to treat arrhythmias during anesthesia, it should be used with extreme caution, usually with constant monitoring of the ECG and central venous pressure.

CONTRAINDICATIONS

Propayerst Plus (Propranolol Hydrochloride) is contraindicated in 1) cardiogenic shock; 2) sinus bradycardia and greater than first-degree block; 3) bronchial asthma; and 4) in patients with known hypersensitivity to Propayerst Plus (Propranolol Hydrochloride) hydrochloride.

WARNINGS

Cardiac Failure

Sympathetic stimulation may be a vital component supporting circulatory function in patients with congestive heart failure, and its inhibition by beta blockade may precipitate more severe failure. Although beta-blockers should be avoided in overt congestive heart failure, some have been shown to be highly beneficial when used with close follow-up in patients with a history of failure who are well compensazted and are receiving additional therapies, including diiuretics as needed. Beta-adrenergic blocking agents do not abolish the inotropic action of digitalis on heart muscle.

Nonallergic Bronchospasm (e.g., Chronic Bronchitis, Emphysema)

In general, patients with bronchospastic lung disease should not receive beta blockers. Propayerst Plus (Propranolol Hydrochloride) should be administered with caution in this setting since it may block bronchodilation produced by endogenous and exogenous catecholamine stimulation of beta-receptors.

Major Surgery

The necessity or desirability of withdrawal of beta-blocking therapy prior to major surgery is controversial. It should be noted, however, that the impaired ability of the heart to respond to reflex adrenergic stimuli in propranolol-treated patients might augment the risks of general anesthesia and surgical procedures.

Propayerst Plus (Propranolol Hydrochloride) is a competitive inhibitor of beta-receptor agonists, and its effects can be reversed by administration of such agents, e.g., dobutamine or isoproterenol. However, such patients may be subject to protracted severe hypotension.

Diabetes and Hypoglycemia

Beta-adrenergic blockade may prevent the appearance of certain premonitory signs and symptoms (pulse rate and pressure changes) of acute hypoglycemia, especially in labile insulin-dependent diabetics. In these patients, it may be more difficult to adjust the dosage of insulin.

Propayerst Plus (Propranolol Hydrochloride) therapy, particularly in infants and children, diabetic or not, has been associated with hypoglycemia especially during fasting, as in preparation for surgery. Hypoglycemia has been reported after prolonged physical exertion and in patients with renal insufficiency.

Thyrotoxicosis

Beta-adrenergic blockade may mask certain clinical signs of hyperthyroidism. Therefore, abrupt withdrawal of Propayerst Plus (Propranolol Hydrochloride) may be followed by an exacerbation of symptoms of hyperthyroidism, including thyroid storm. Propayerst Plus (Propranolol Hydrochloride) may change thyroid-function tests, increasing T_4 and reverse T_3, and decreasing T_3.

Wolff-Parkinson-White Syndrome

Beta-adrenergic blockade in patients with Wolff-Parkinson-White syndrome and tachycardia has been associated with severe bradycardia requiring treatment with a pacemaker. In one case this resulted after an initial 5 mg dose of intravenous Propayerst Plus (Propranolol Hydrochloride).

PRECAUTIONS

General

Propayerst Plus (Propranolol Hydrochloride) should be used with caution in patients with impaired hepatic or renal function.

Propayerst Plus (Propranolol Hydrochloride) is not indicated for the treatment of hypertensive emergencies.

Beta-adrenergic receptor blockade can cause reduction of intraocular pressure. Patients should be told that Propayerst Plus (Propranolol Hydrochloride) might interfere with the glaucoma screening test. Withdrawal may lead to a return of elevated intraocular pressure.

Risk of anaphylactic reaction. While taking beta blockers, patients with a history of severe anaphylactic reaction to a variety of allergens may be more reactive to repeated challenge, either accidental, diagnostic, or therapeutic. Such patients may be unresponsive to the usual doses of epinephrine used to treat allergic reaction.

Angina Pectoris

There have been reports of exacerbation of angina and, in some cases, myocardial infarction, following abrupt discontinuance of Propayerst Plus (Propranolol Hydrochloride) therapy. Therefore, when discontinuance of Propayerst Plus (Propranolol Hydrochloride) is planned, the dosage should be gradually reduced over at least a few weeks, and the patient should be cautioned against interruption or cessation of therapy without a physician’s advice. If Propayerst Plus (Propranolol Hydrochloride) therapy is interrupted and exacerbation of angina occurs, it is usually advisable to reinstitute Propayerst Plus (Propranolol Hydrochloride) therapy and take other measures appropriate for the management of angina pectoris. Since coronary artery disease may be unrecognized, it may be prudent to follow the above advice in patients considered at risk of having occult atherosclerotic heart disease who are given Propayerst Plus (Propranolol Hydrochloride) for other indications.

Clinical Laboratory Tests

In patients with hypertension, use of Propayerst Plus (Propranolol Hydrochloride) has been associated with elevated levels of serum potassium, serum transaminases and alkaline phosphatase. In severe heart failure, the use of Propayerst Plus (Propranolol Hydrochloride) has been associated with increases in Blood Urea Nitrogen.

Drug Interactions

Caution should be exercised when Propayerst Plus (Propranolol Hydrochloride) is administered with drugs that have an effect on CYP2D6, 1A2, or 2C19 metabolic pathways. Co-administration of such drugs with Propayerst Plus (Propranolol Hydrochloride) may lead to clinically relevant drug interactions and changes in its efficacy and/or toxicity (see CLINICAL PHARMACOLOGY, DRUG INTERACTIONS.

Cardiovascular Drugs

Antirrhythmics

Propafenone has negative inotropic and beta-blocking properties that can be additive to those of Propayerst Plus (Propranolol Hydrochloride).

Quinidine increases the concentration of Propayerst Plus (Propranolol Hydrochloride) and produces a greater degree of clinical beta-blockade and may cause postural hypotension.

Disopyramide is a Type I antiarrhythmic drug with potent negative inotropic and chronotropic effects and has been associated with severe bradycardia, asystole and heart failure when administered with Propayerst Plus (Propranolol Hydrochloride).

Amiodarone is an antiarrhythmic agent with negative chronotropic properties that may be additive to those seen with Propayerst Plus (Propranolol Hydrochloride).

The clearance of lidocaine is reduced when administered with Propayerst Plus (Propranolol Hydrochloride). Lidocaine toxicity has been reported following co-administration with Propayerst Plus (Propranolol Hydrochloride).

Caution should be exercised when administering Propayerst Plus (Propranolol Hydrochloride) with drugs that slow A-V nodal conduction, e.g., digitalis, lidocaine and calcium channel blockers.

Calcium Channel Blockers

Caution should be exercised when patients receiving a beta-blocker are administered a calcium-channel-blocking drug with negative inotropic and/or chronotropic effects. Both agents may depress myocardial contractility or atrioventricular conduction.

There have been reports of significant bradycardia, heart failure, and cardiovascular collapse with concurrent use of verapamil and beta‑blockers.

Co-administration of Propayerst Plus (Propranolol Hydrochloride) and diltiazem in patients with cardiac disease has been associated with bradycardia, hypotension, high degree heart block, and heart failure.

ACE Inhibitors

When combined with beta-blockers, ACE inhibitors can cause hypotension, particularly in the setting of acute myocardial infarction.

ACE inhibitors have been reported to increase bronchial hyperreactivity when administered with Propayerst Plus (Propranolol Hydrochloride).

The antihypertensive effects of clonidine may be antagonized by beta-blockers. Propayerst Plus (Propranolol Hydrochloride) should be administered cautiously to patients withdrawing from clonidine.

Alpha-blockers

Prazosin has been associated with prolongation of first dose hypotension in the presence of beta-blockers.

Postural hypotension has been reported in patients taking both beta-blockers and terazosin or doxazosin.

Reserpine

Patients receiving catecholamine-depleting drugs, such as reserpine, with Propayerst Plus (Propranolol Hydrochloride) should be closely observed for excess reduction of resting sympathetic nervous activity, which may result in hypotension, marked bradycardia, vertigo, syncopal attacks, or orthostatic hypotension. Administration of reserpine with Propayerst Plus (Propranolol Hydrochloride) may also potentiate depression.

Inotropic Agents

Patients on long-term therapy with Propayerst Plus (Propranolol Hydrochloride) may experience uncontrolled hypertension if administered epinephrine as a consequence of unopposed alpha-receptor stimulation. Epinephrine is therefore not indicated in the treatment of Propayerst Plus (Propranolol Hydrochloride) overdose.

Isoproterenol and Dobutamine

Propranolol is a competitive inhibitor of beta-receptor agonists, and its effects can be reversed by administration of such agents, e.g., dobutamine or isoproterenol. Also, Propayerst Plus (Propranolol Hydrochloride) may reduce sensitivity to dobutamine stress echocardiography in patients undergoing evaluation for myocardial ischemia.

Non-Cardiovascular Drugs

Non-Steroidal Anti-Inflammatory Drugs

Non-steroidal anti-inflammatory drugs (NSAIDs) have been reported to blunt the antihypertensive effect of beta-adrenoreceptor blocking agents.

Administration of indomethacin with Propayerst Plus (Propranolol Hydrochloride) may reduce the efficacy of Propayerst Plus (Propranolol Hydrochloride) in reducing blood pressure and heart rate.

Antidepressants

The hypotensive effects of MAO inhibitors or tricyclic antidepressants may be exacerbated when administered with beta-blockers by interfering with the beta blocking activity of Propayerst Plus (Propranolol Hydrochloride).

Anesthetic Agents

Methoxyflurane and trichloroethylene may depress myocardial contractility when administered with Propayerst Plus (Propranolol Hydrochloride).

Warfarin

Administration of Propayerst Plus (Propranolol Hydrochloride) with warfarin increases the concentration of warfarin. Therefore, the prothrombin time should be monitored.

Neuroleptic Drugs

Hypotension and cardiac arrest have been reported with the concomitant use of Propayerst Plus (Propranolol Hydrochloride) and haloperidol.

Thyroxine

Thyroxine may result in a lower than expected T3 concentration when used concomitantly with Propayerst Plus (Propranolol Hydrochloride).

Carcinogenesis, Mutagenesis, Impairment of Fertility

In dietary administration studies in which mice and rats were treated with Propayerst Plus (Propranolol Hydrochloride) hydrochloride for up to 18 months at doses of up to 150 mg/kg/day, there was no evidence of drug-related tumorigenesis. On a body surface area basis, this dose in the mouse and rat is, respectively, about equal to and about twice the maximum recommended human oral daily dose (MRHD) of 640 mg Propayerst Plus (Propranolol Hydrochloride) hydrochloride. In a study in which both male and female rats were exposed to Propayerst Plus (Propranolol Hydrochloride) hydrochloride in their diets at concentrations of up to 0.05% (about 50 mg/kg body weight and less than the MRHD), from 60 days prior to mating and throughout pregnancy and lactation for two generations, there were no effects on fertility. Based on differing results from Ames Tests performed by different laboratories, there is equivocal evidence for a genotoxic effect of Propayerst Plus (Propranolol Hydrochloride) hydrochloride in bacteria (S. typhimurium strain TA 1538).

Pregnancy

Pregnancy Category C

In a series of reproductive and developmental toxicology studies, Propayerst Plus (Propranolol Hydrochloride) hydrochloride was given to rats by gavage or in the diet throughout pregnancy and lactation. At doses of 150 mg/kg/day, but not at doses of 80 mg/kg/day (equivalent to the MRHD on a body surface area basis), treatment was associated with embryotoxicity (reduced litter size and increased resorption rates) as well as neonatal toxicity (deaths). Propayerst Plus (Propranolol Hydrochloride) hydrochloride also was administered (in the feed) to rabbits (throughout pregnancy and lactation) at doses as high as 150 mg/kg/day (about 5 times the maximum recommended human oral daily dose). No evidence of embryo or neonatal toxicity was noted.

There are no adequate and well-controlled studies in pregnant women. Intrauterine growth retardation has been reported for neonates whose mothers received Propayerst Plus (Propranolol Hydrochloride) hydrochloride during pregnancy. Neonates whose mothers received Propayerst Plus (Propranolol Hydrochloride) hydrochloride at parturition have exhibited bradycardia, hypoglycemia, and respiratory depression. Adequate facilities for monitoring such infants at birth should be available. Propayerst Plus (Propranolol Hydrochloride) should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.

Nursing Mothers

Propayerst Plus (Propranolol Hydrochloride) is excreted in human milk. Caution should be exercised when Propayerst Plus (Propranolol Hydrochloride) is administered to a nursing woman.

Pediatric Use

Safety and effectiveness of Propayerst Plus (Propranolol Hydrochloride) in pediatric patients have not been established.

Geriatric Use

Clinical studies of intravenous Propayerst Plus (Propranolol Hydrochloride) did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Elderly subjects have decreased clearance and a longer mean elimination half‑life. These findings suggest that dose adjustment of Propayerst Plus (Propranolol Hydrochloride) injection may be required for elderly patients. In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of the decreased hepatic, renal or cardiac function, and of concomitant disease or other drug therapy.

Hepatic Insufficiency

Propayerst Plus (Propranolol Hydrochloride) is extensively metabolized by the liver. Compared to normal subjects, patients with chronic liver disease have decreased clearance of Propayerst Plus (Propranolol Hydrochloride), increased volume of distribution, decreased protein-binding and considerable variation in half life. Consideration should be given to lowering the dose of intravenously administered Propayerst Plus (Propranolol Hydrochloride) in patients with hepatic insufficiency.

ADVERSE REACTIONS

In a series of 225 patients, there were 6 deaths. Cardiovascular events (hypotension, congestive heart failure, bradycardia, and heart block) were the most common. The only other event reported by more than one patient was nausea.

Other adverse events for intravenous Propayerst Plus (Propranolol Hydrochloride), reported during post-marketing surveillance include cardiac arrest, dyspnea, and cutaneous ulcers.

The following adverse events have been reported with use of formulations of sustained- or immediate-release oral Propayerst Plus (Propranolol Hydrochloride) and may be expected with intravenous Propayerst Plus (Propranolol Hydrochloride).

Cardiovascular

Bradycardia; congestive heart failure; intensification of AV block; hypotension; paresthesia of hands; thrombocytopenic purpura; arterial insufficiency, usually of the Raynaud type.

Central Nervous System

Light-headedness; mental depression manifested by insomnia, lassitude, weakness, fatigue; reversible mental depression progressing to catatonia; visual disturbances; hallucinations; vivid dreams; an acute reversible syndrome characterized by disorientation for time and place, short-term memory loss, emotional lability, slightly clouded sensorium, and decreaseed performance on neuropsychometrics. For immediate-release formulations, fatigue, lethargy, and vivid dreams appear dose-related.

Gastrointestinal

Nausea, vomiting, epigastric distress, abdominal cramping, diarrhea, constipation, mesenteric arterial thrombosis, ischemic colitis.

Allergic

Pharyngitis and agranulocytosis; erythematous rash, fever combined with aching and sore throat; laryngospasm, and respiratory distress.

Respiratory

Bronchospasm.

Hematologic

Agranulocytosis, nonthrombocytopenic purpura, thrombocytopenic purpura.

Autoimmune

In extremely rare instances, systemic lupus erythematosus has been reported.

Miscellaneous

Alopecia, LE-like reactions, psoriform rashes, dry eyes, male impotence, and Peyronie's disease have been reported rarely. Oculomucocutaneous reactions involving the skin, serous membranes and conjunctivae reported for a beta-blocker (practolol) have not been associated with Propayerst Plus (Propranolol Hydrochloride).

To report SUSPECTED ADVERSE REACTIONS, contact West-ward Pharmaceutical Corp. at 1-877-233-2001 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

OVERDOSAGE

Propayerst Plus (Propranolol Hydrochloride) is not significantly dialyzable. In the event of overdose or exaggerated response, the following measures should be employed:

Hypotension and bradycardia have been reported following Propayerst Plus (Propranolol Hydrochloride) overdose and should be treated appropriately. Glucagon can exert potent inotropic and chronotropic effects and may be particularly useful for the treatment of hypotension or depressed myocardial function after a Propayerst Plus (Propranolol Hydrochloride) overdose. Glucagon should be administered as 50-150 mcg/kg intravenously followed by continuous drip of 1-5 mg/hour for positive chronotropic effect. Isoproterenol, dopamine, or phosphodiesterase inhibitors may also be useful. Epinephrine, however, may provoke uncontrolled hypertension. Bradycardia can be treated with atropine or isoproterenol. Serious bradycardia may require temporary cardiac pacing.

The electrocardiogram, pulse, blood pressure, neurobehavioral status and intake and output balance must be monitored. Isoproterenol and aminophylline may be useful for bronchospasm.

DOSAGE & ADMINISTRATION

Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

The usual dose is 1 to 3 mg administered under careful monitoring, such as electrocardiography and central venous pressure. The rate of administration should not exceed 1 mg (1 mL) per minute to diminish the possibility of lowering blood pressure and causing cardiac standstill. Sufficient time should be allowed for the drug to reach the site of action even when a slow circulation is present. If necessary, a second dose may be given after two minutes. Thereafter, additional drug should not be given in less than four hours. Additional Propayerst Plus (Propranolol Hydrochloride) hydrochloride should not be given when the desired alteration in rate or rhythm is achieved.

Transfer to oral therapy as soon as possible.

HOW SUPPLIED

Each mL contains 1 mg of Propayerst Plus (Propranolol Hydrochloride) Hydrochloride, USP in Water for Injection, USP. The pH is adjusted with anhydrous Citric Acid, USP. Supplied as: 1 mL vials in boxes of 10 (NDC 0143-9872-10).

Store at 20° to 25°C (68° to 77°F). Protect from freezing or excessive heat.

Manufactured by: HIKMA FARMACÊUTICA (PORTUGAL), S.A.

Estrada do Rio da Mó, 8, 8A e 8B – Fervença – 2705-906 Terrugem SNT, PORTUGAL

Distributed by: WEST-WARD PHARMACEUTICAL CORP.

Eatontown, NJ 07724 USA

Rev.: 05/2015

PIN166-WES/4