hydrochlorothiazide and benazepril

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Lotensin HCT, |hydrochlorothiazide and benazepril

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hydrochlorothiazide and benazepril

Generic Name: hydrochlorothiazide and benazepril (hye droe klor oh THYE a zide and beh NAY zah prill)
Brand Names: Lotensin HCT

What is hydrochlorothiazide and benazepril?

Hydrochlorothiazide is a thiazide diuretic (water pill). It increases the amount of salt and water you lose in your urine. Hydrochlorothiazide is used to lower blood pressure and to decrease edema (swelling).

Benazepril is in a class of drugs called angiotensin-converting-enzyme inhibitors (ACE inhibitors). Benazepril is used to lower blood pressure and to relieve the symptoms of congestive heart failure, including shortness of breath and swelling of the legs.

Hydrochlorothiazide and benazepril is used to treat hypertension (high blood pressure).

Hydrochlorothiazide and benazepril may also be used for purposes other than those listed in this medication guide.

What is the most important information I should know about hydrochlorothiazide and benazepril?

Benazepril is in the FDA pregnancy category D. This means that benazepril is known to harm an unborn baby. When used during the second and third trimesters of pregnancy, benazepril can cause injury and even death to the developing fetus. Do not take hydrochlorothiazide and benazepril if you are pregnant.

Benazepril may increase the risk of dangerous allergic reactions. Before taking hydrochlorothiazide and benazepril, tell your doctor if you have ever had an allergic reaction that involved swelling of your lips, face, tongue, or throat or difficulty breathing. Seek emergency medical attention if you develop any of these symptoms while taking hydrochlorothiazide and benazepril.

Use caution when driving, operating machinery, or performing other hazardous activities. Hydrochlorothiazide and benazepril may cause dizziness or drowsiness. If you experience dizziness or drowsiness, avoid these activities. Also use caution when rising from a sitting or lying position.

Who should not take hydrochlorothiazide and benazepril?

Do not take hydrochlorothiazide and benazepril if you have an allergy to sulfa-based drugs such as sulfa antibiotics. You may have an allergic reaction to hydrochlorothiazide.

Benazepril may increase the risk of dangerous allergic reactions. Before taking hydrochlorothiazide and benazepril, tell your doctor if you have ever had an allergic reaction that involved swelling of your lips, face, tongue, or throat or difficulty breathing. Seek emergency medical attention if you develop any of these symptoms while taking hydrochlorothiazide and benazepril.

Before taking hydrochlorothiazide and benazepril, tell your doctor if you

  • have diabetes,

  • have gout,

  • have a collagen vascular disease such as systemic lupus erythematosus or scleroderma,

  • have pancreatitis;

  • have kidney disease,
  • have liver disease,
  • have a blood or bone marrow disease,

  • have any type of heart disease or have had a stroke,

  • are taking salt substitutes, potassium supplements (e.g., K-Dur, Klor-Con), or potassium-sparing diuretics such as amiloride (Midamor), triamterene (Dyrenium, Dyazide, Maxzide), or spironolactone (Aldactone); or

  • are on a salt-restricted diet or have high levels of potassium in your blood.

You may not be able to take hydrochlorothiazide and benazepril, or you may require a dosage adjustment or special monitoring during treatment if you have any of the conditions listed above.

Benazepril is in the FDA pregnancy category D. This means that benazepril is known to harm an unborn baby. When used during the second and third trimesters of pregnancy, benazepril can cause injury and even death to the developing fetus. Do not take hydrochlorothiazide and benazepril if you are pregnant. Hydrochlorothiazide passes into breast milk and may harm a nursing infant. It is not know whether benazepril passes into breast milk. Do not take this medication without first talking to your doctor if you are breast-feeding a baby. If you are over 60 years of age, you may be more likely to experience side effects from hydrochlorothiazide and benazepril. Your doctor may prescribe a lower dose of this medication.

How should I take hydrochlorothiazide and benazepril?

Take hydrochlorothiazide and benazepril exactly as directed by your doctor. If you do not understand these directions, ask your pharmacist, nurse, or doctor to explain them to you.

Take each dose with a full glass of water. Do not stop taking this medication without first talking to your doctor. If you stop taking your medication, your condition could become worse. Store hydrochlorothiazide and benazepril at room temperature away from moisture and heat.

What happens if I miss a dose?

Take the missed dose as soon as you remember. However, if it is almost time for your next dose, skip the missed dose and take only your next regularly scheduled dose. Do not take a double dose of this medication.

What happens if I overdose?

Seek emergency medical attention.

Symptoms of a hydrochlorothiazide and benazepril overdose include increased urination, nausea, vomiting, diarrhea, dizziness, fainting, weakness, fatigue, and unconsciousness.

What should I avoid while taking hydrochlorothiazide and benazepril?

Use caution when driving, operating machinery, or performing other hazardous activities. Hydrochlorothiazide and benazepril may cause dizziness or drowsiness. If you experience dizziness or drowsiness, avoid these activities. Also use caution when rising from a sitting or lying position. Use alcohol cautiously. Alcohol may further lower blood pressure, causing increased drowsiness and dizziness while you are taking hydrochlorothiazide and benazepril.

Avoid a diet high in salt. Too much salt may cause your body to retain water and may decrease the effects of hydrochlorothiazide. Ask your doctor or nurse about low-salt diet alternatives.

Do not use salt substitutes or potassium supplements while taking benazepril and hydrochlorothiazide without first talking to your doctor . These products could cause potassium levels in your blood to become dangerously high.

Avoid prolonged exposure to sunlight. Hydrochlorothiazide and benazepril may increase the sensitivity of your skin to sunlight. Use a sunscreen and wear protective clothing when exposure to the sun is unavoidable.

Heavy sweating, vomiting, diarrhea, or other causes of fluid loss may lead to very low blood pressure, dizziness, and fainting during therapy with hydrochlorothiazide and benazepril. Maintain proper fluid intake to prevent dehydration and related adverse effects.

Hydrochlorothiazide and benazepril side effects

If you experience any of the following serious side effects, stop taking hydrochlorothiazide and benazepril and seek emergency medical attention:
  • an allergic reaction (difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives);

  • fainting spells;

  • unusual fatigue or abnormal bleeding or bruising;

  • yellow skin or eyes;

  • confusion;

  • fever, chills, or a sore throat;

  • little or no urine;

  • irregular heartbeats; or

  • increased swelling.

Other, less serious side effects may be more likely to occur. Continue to take hydrochlorothiazide and benazepril and talk to your doctor if you experience

  • dizziness or lightheadedness;

  • headache;

  • fatigue;

  • tingling or numbness in your arms, legs, hands, or feet;

  • excessive urination;

  • muscle weakness or cramps;

  • increased hunger or thirst;

  • nausea, diarrhea, constipation, decreased appetite, or changes in taste;

  • sensitivity to sunlight;

  • dry, tickling cough;

  • anxiety or depression; or

  • itching, rash, or increased sweating.

Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.

What other drugs will affect hydrochlorothiazide and benazepril?

Before taking hydrochlorothiazide and benazepril, tell your doctor if you are taking any of the following drugs:

  • a potassium supplement such as K-Dur, Klor-Con, and others;

  • a salt substitute that contains potassium;

  • another diuretic (water pill) especially triamterene (Dyrenium, Maxzide, Dyazide), spironolactone (Aldactone), or amiloride (Midamor);

  • cholestyramine (Questran) or colestipol (Colestid);

  • a nonsteroidal anti-inflammatory drug (NSAID) such as ibuprofen (Motrin, Advil), ketoprofen (Orudis, Orudis KT, Oruvail), naproxen (Naprosyn, Anaprox, Aleve), diclofenac (Cataflam, Voltaren), etodolac (Lodine), fenoprofen (Nalfon), flurbiprofen (Ansaid), indomethacin (Indocin), ketorolac (Toradol), mefenamic acid (Ponstel), nabumetone (Relafen), oxaprozin (Daypro), piroxicam (Feldene), sulindac (Clinoril), or tolmetin (Tolectin);

  • an oral diabetes medication such as glipizide (Glucotrol), glyburide (Micronase, Glynase, Diabeta), chlorpropamide (Diabinese), tolazamide (Tolinase), tolbutamide (Orinase), and others;

  • tetracycline (Sumycin, others);

  • lithium (Lithane, Lithobid, Eskalith, others);

  • a calcium channel blocker such as amlodipine (Norvasc), diltiazem (Cardizem, Dilacor XR, Tiazac), nifedipine (Adalat, Procardia), verapamil (Calan, Verelan, Isoptin), and others;

  • doxazosin (Cardura), prazosin (Minipress), or terazosin (Hytrin);

  • reserpine, guanadrel (Hylorel), or guanethidine (Ismelin);

  • a nitrate such as nitroglycerin (Nitrostat, Transderm-Nitro, Nitro-Dur, Nitro-Bid, Minitran, others), isosorbide mononitrate (Imdur, ISMO), or isosorbide dinitrate (Isordil, Sorbitrate);

  • a pain reliever such as codeine, morphine (MS Contin, MSIR, Roxanol, others), propoxyphene (Darvocet, Darvon, Wygesic), oxycodone (Percocet, Percodan), meperidine (Demerol), and others;

  • a barbiturate such as phenobarbital (Luminal, Solfoton), amobarbital (Amytal), secobarbital (Seconal), and butabarbital (Butisol); or

  • a steroid medicine such as cortisone (Cortone), dexamethasone (Decadron, Hexadrol), betamethasone (Celestone), hydrocortisone (Cortef, Hydrocortone), prednisone (Orasone, Deltasone), prednisolone (Delta Cortef, Prelone), methylprednisolone (Medrol), and others.

You may not be able to take hydrochlorothiazide and benazepril, or you may require a dosage adjustment or special monitoring during your treatment if you are taking any of the medicines listed above.

Drugs other than those listed here may also interact with hydrochlorothiazide and benazepril or affect your condition. Talk to your doctor and pharmacist before taking any prescription or over-the-counter medicines.

Where can I get more information?

  • Your pharmacist has additional information about hydrochlorothiazide and benazepril written for health professionals that you may read.

What does my medication look like?

Hydrochlorothiazide and benazepril is available with a prescription under the brand name Lotensin HCT. Other brand or generic formulations may also be available. Ask your pharmacist any questions you have about this medication, especially if it is new to you.

Benazepril/hydrochlorothiazide strengths are as follows:

  • Lotensin HCT 5 mg/6.25 mg--white, oblong, scored tablets

  • Lotensin HCT 10 mg/12.5 mg--light-pink, oblong, scored tablets

  • Lotensin HCT 20 mg/12.5 mg--grayish-violet, oblong, scored tablets

  • Lotensin HCT 20 mg/25 mg--red, oblong, scored tablets

  • Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed.
  • Every effort has been made to ensure that the information provided by Cerner Multum, Inc. ("Multum") is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Multum does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Multum"s drug information does not endorse drugs, diagnose patients or recommend therapy. Multum"s drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.
Copyright 1996-2006 Cerner Multum, Inc. Version: 3.05. Revision Date: 2/13/04 4:03:58 PM.



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