Hydrochlorothiazide 25mg Tablets

Manufacturer UNICHEM Active Ingredient Hydrochlorothiazide(hye droe klor oh THYE a zide) Pronunciation hye droe klor oh THYE a zide
It is used to treat high blood pressure.It is used to get rid of extra fluid.It may be given to you for other reasons. Talk with the doctor.
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Drug Class
Antihypertensive, Diuretic
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Pharmacologic Class
Thiazide Diuretic
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Pregnancy Category
B
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FDA Approved
Mar 1959
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DEA Schedule
Not Controlled

Overview

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What is this medicine?

Hydrochlorothiazide is a 'water pill' (diuretic) that helps your body get rid of extra salt and water. This helps to lower your blood pressure and reduce swelling (edema).
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How to Use This Medicine

Taking Your Medication Correctly

To get the most benefit from your medication, take it exactly as directed by your doctor. Carefully read all the information provided with your prescription, and follow the instructions closely.

Continuing Your Medication

Continue taking your medication as prescribed by your doctor or healthcare provider, even if you start to feel better. It's essential to maintain your treatment regimen to achieve the best results.

Managing Potential Side Effects

This medication may increase your urine production, which can lead to more frequent trips to the bathroom. To minimize sleep disturbances, try to avoid taking your medication too close to bedtime.

Oral Suspension Instructions

You can take the oral suspension with or without food. Before using, shake the bottle well to ensure the medication is evenly mixed. When measuring your dose, use the provided measuring device or ask your pharmacist for a suitable alternative.

Storing and Disposing of Your Medication

To maintain the effectiveness and safety of your medication:

Store it at room temperature, away from direct light.
Keep it in a dry place, avoiding storage in a bathroom.
* Ensure the lid is tightly closed when not in use.

Missing a Dose

If you miss a dose, take it as soon as you remember. However, if it's close to the time for your next scheduled dose, skip the missed dose and resume your regular dosing schedule. Do not take two doses at the same time or take extra doses to make up for the missed one.
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Lifestyle & Tips

  • Take this medication exactly as prescribed, usually once daily in the morning to avoid nighttime urination.
  • Do not stop taking this medication without talking to your doctor, even if you feel well.
  • Limit alcohol intake, as it can increase the blood pressure-lowering effect and risk of dizziness.
  • Maintain a balanced diet. Your doctor may advise you on potassium intake (e.g., eating potassium-rich foods or taking potassium supplements) if your potassium levels are low.
  • Avoid excessive sun exposure and use sunscreen, as this medication can make your skin more sensitive to the sun.
  • Regularly monitor your blood pressure at home if advised by your doctor.
  • Stay hydrated, especially in hot weather or during exercise, but avoid excessive fluid intake unless directed by your doctor.

Dosing & Administration

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Adult Dosing

Standard Dose: 25 mg orally once daily
Dose Range: 12.5 - 50 mg

Condition-Specific Dosing:

hypertension: Initial: 12.5-25 mg once daily; Maintenance: 12.5-50 mg once daily. Doses >50 mg/day generally do not provide additional benefit and increase risk of adverse effects.
edema: Initial: 25-100 mg once daily or intermittently; Maintenance: 25-200 mg/day in 1-2 divided doses or intermittently.
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Pediatric Dosing

Neonatal: Not established
Infant: Not established (use with caution, dose based on weight, e.g., 1-2 mg/kg/day in 1-2 divided doses)
Child: 1-2 mg/kg/day orally in 1-2 divided doses; Max: 3 mg/kg/day or 100 mg/day
Adolescent: 1-2 mg/kg/day orally in 1-2 divided doses; Max: 3 mg/kg/day or 100 mg/day (often adult dosing applies for hypertension)
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Dose Adjustments

Renal Impairment:

Mild: No adjustment needed (CrCl > 50 mL/min)
Moderate: Use with caution; may be less effective (CrCl 30-50 mL/min). Consider lower doses.
Severe: Contraindicated or ineffective (CrCl < 30 mL/min). Loop diuretics are generally preferred.
Dialysis: Not removed by hemodialysis. Contraindicated in anuria.

Hepatic Impairment:

Mild: No specific adjustment, but use with caution.
Moderate: Use with caution; electrolyte imbalances may precipitate hepatic coma.
Severe: Use with caution; electrolyte imbalances may precipitate hepatic coma.

Pharmacology

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Mechanism of Action

Hydrochlorothiazide is a thiazide diuretic that inhibits the reabsorption of sodium and chloride ions in the distal convoluted tubule of the nephron. This action leads to increased excretion of sodium, chloride, and water, as well as potassium and magnesium. It also decreases calcium excretion. The antihypertensive effect is initially due to a decrease in plasma volume and cardiac output, followed by a decrease in peripheral vascular resistance with chronic use.
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Pharmacokinetics

Absorption:

Bioavailability: 60-80%
Tmax: 2-5 hours
FoodEffect: Food may increase the extent of absorption.

Distribution:

Vd: 0.8 L/kg
ProteinBinding: 40-68%
CnssPenetration: Limited

Elimination:

HalfLife: 5.6-14.8 hours (mean 6-15 hours)
Clearance: Not available (primarily renal excretion)
ExcretionRoute: Renal (unchanged drug)
Unchanged: Approximately 50-70%
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Pharmacodynamics

OnsetOfAction: Approximately 2 hours
PeakEffect: 4-6 hours
DurationOfAction: 6-12 hours

Safety & Warnings

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Side Effects

Urgent Side Effects: Seek Medical Help Right Away

Although rare, some people may experience severe and potentially life-threatening side effects while taking this medication. If you notice any of the following symptoms, contact your doctor or seek immediate medical attention:

Signs of an allergic reaction, such as:
+ Rash or hives
+ Itching or red, swollen, blistered, or peeling skin (with or without fever)
+ Wheezing or tightness in the chest or throat
+ Difficulty breathing, swallowing, or talking
+ Unusual hoarseness or swelling of the mouth, face, lips, tongue, or throat
Signs of high blood sugar, including:
+ Confusion or feeling sleepy
+ Unusual thirst or hunger
+ Frequent urination
+ Flushing or fast breathing
+ Breath that smells like fruit
Signs of fluid and electrolyte problems, such as:
+ Mood changes or confusion
+ Muscle pain or weakness
+ Abnormal heartbeat or severe dizziness
+ Increased thirst or seizures
+ Feeling extremely tired or weak
+ Decreased appetite or inability to urinate
+ Changes in urine output or dry mouth
+ Dry eyes or severe stomach upset
Signs of pancreatitis (pancreas problems), including:
+ Severe stomach pain
+ Severe back pain
+ Severe stomach upset or vomiting
Signs of kidney problems, such as:
+ Inability to urinate or changes in urine output
+ Blood in the urine or significant weight gain
+ Dark urine or yellow skin and eyes
Fever, chills, or sore throat
Unexplained bruising or bleeding
Feeling extremely tired or weak
Abnormal sensations, such as burning, numbness, or tingling
Shortness of breath
Restlessness
Difficulty getting or maintaining an erection

Eye Problems:

This medication can cause certain eye problems, which may lead to permanent vision loss if left untreated. If you experience any of the following symptoms, contact your doctor immediately:

Changes in vision
Eye pain (usually occurring within hours to weeks of starting the medication)

Skin Cancer Risk:

Rarely, people taking hydrochlorothiazide have developed certain types of skin cancer. To minimize this risk, protect your skin from the sun and follow your doctor's recommendations for skin checks. If you notice any changes in the color or size of a mole, or any new or changing skin lumps or growths, contact your doctor right away.

Other Side Effects:

Most people do not experience significant side effects, but some may occur. If you are bothered by any of the following side effects or if they persist, contact your doctor:

Constipation, diarrhea, stomach upset, vomiting, or decreased appetite
Stomach cramps
Dizziness, tiredness, or weakness
Headache

Reporting Side Effects:

If you have questions or concerns about side effects, contact your doctor. You can also report side effects to the FDA at 1-800-332-1088 or online at https://www.fda.gov/medwatch.
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Seek Immediate Medical Attention If You Experience:

  • Severe dizziness or fainting (signs of low blood pressure)
  • Unusual tiredness, muscle weakness, or muscle cramps (signs of low potassium or magnesium)
  • Excessive thirst, dry mouth, nausea, vomiting (signs of dehydration or electrolyte imbalance)
  • Sudden, severe joint pain, especially in the big toe (signs of gout)
  • Yellowing of skin or eyes (jaundice)
  • Signs of an allergic reaction: rash, itching, swelling (especially of face/tongue/throat), severe dizziness, trouble breathing.
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Before Using This Medicine

Before Taking This Medication: Important Information to Share with Your Doctor

It is essential to inform your doctor about the following:

Any allergies you have, including allergies to this medication, its components, or other substances, such as foods or drugs. Be sure to describe the symptoms you experienced.
A known sulfa allergy.
Difficulty urinating or inability to pass urine.
Current use of dofetilide or lithium.

This list is not exhaustive, and it is crucial to discuss all your medications (prescription, over-the-counter, natural products, and vitamins) and health issues with your doctor and pharmacist. They will help determine if it is safe to take this medication with your other medications and health conditions. Never start, stop, or adjust the dosage of any medication without first consulting your doctor.
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Precautions & Cautions

Important Information About Your Medication

It is crucial that you inform all of your healthcare providers, including doctors, nurses, pharmacists, and dentists, that you are taking this medication. This will help ensure that you receive the best possible care.

Caution When Performing Daily Activities

Until you know how this medication affects you, avoid driving and other tasks that require you to be alert. To minimize the risk of dizziness or fainting, get up slowly from a sitting or lying down position, and be cautious when climbing stairs.

Monitoring Your Health

Follow your doctor's instructions for regular blood tests and other laboratory evaluations. This medication may cause increases in cholesterol and triglyceride levels, so it is essential to discuss your lipid profile with your doctor if you have high cholesterol or triglycerides.

Managing Related Health Conditions

If you have diabetes, you will need to closely monitor your blood sugar levels. Additionally, check your blood pressure as directed by your doctor. This medication may affect certain laboratory tests, so be sure to inform all of your healthcare providers and laboratory personnel that you are taking this medication.

Interactions with Other Medications and Substances

If you have high blood pressure, consult with your doctor before taking over-the-counter (OTC) products that may increase blood pressure, such as cough or cold medications, diet pills, stimulants, non-steroidal anti-inflammatory drugs (NSAIDs) like ibuprofen or naproxen, and certain natural products or aids.

Understanding the Medication's Effects

This medication is a potent diuretic, which means it can cause your body to lose excess fluid and electrolytes (such as potassium). Your doctor will closely monitor you to adjust the dosage as needed to prevent severe health problems.

Dietary Considerations

If you are on a low-salt or salt-free diet, discuss this with your doctor. Additionally, talk to your doctor before consuming alcohol, marijuana, or other forms of cannabis, or taking prescription or OTC medications that may cause drowsiness.

Managing Potential Side Effects

Inform your doctor if you experience excessive sweating, fluid loss, vomiting, or diarrhea, as these can lead to low blood pressure. If you take cholestyramine or colestipol, consult with your pharmacist about how to take these medications with this drug, and be aware of the potential for gout attacks.

Special Considerations

If you have lupus, this medication may cause your condition to become active or worsen. Report any new or worsening symptoms to your doctor immediately. This medication may also increase your risk of sunburn, so take precautions when spending time outdoors and inform your doctor if you experience sunburn easily.

Age-Related Considerations

If you are 65 or older, use this medication with caution, as you may be more susceptible to side effects.

Pregnancy and Breastfeeding

Inform your doctor if you are pregnant, plan to become pregnant, or are breastfeeding. Your doctor will discuss the benefits and risks of this medication with you, and help you make an informed decision about its use.
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Overdose Information

Overdose Symptoms:

  • Acute volume depletion (dehydration)
  • Electrolyte imbalance (hypokalemia, hyponatremia, hypochloremia)
  • Hypotension (low blood pressure)
  • Dizziness, weakness, confusion
  • Nausea, vomiting
  • Cardiac arrhythmias (due to electrolyte imbalance)

What to Do:

Seek immediate medical attention. Call 911 or your local emergency number. For poison control, call 1-800-222-1222. Management is supportive, focusing on fluid and electrolyte replacement.

Drug Interactions

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Contraindicated Interactions

  • Anuria
  • Hypersensitivity to hydrochlorothiazide or other sulfonamide-derived drugs
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Major Interactions

  • Lithium (increased lithium toxicity due to decreased renal clearance)
  • Nonsteroidal Anti-inflammatory Drugs (NSAIDs) (may reduce diuretic, natriuretic, and antihypertensive effects of thiazides)
  • Digoxin (increased risk of digitalis toxicity due to hypokalemia)
  • Corticosteroids, ACTH (increased risk of electrolyte depletion, particularly hypokalemia)
  • Cholestyramine, Colestipol (may impair absorption of hydrochlorothiazide)
  • Diazoxide (enhanced hyperglycemic and hypotensive effects)
  • Neuromuscular blocking agents (e.g., tubocurarine) (enhanced effect due to hypokalemia)
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Moderate Interactions

  • Antidiabetic agents (insulin, oral hypoglycemics) (may decrease hypoglycemic effect, requiring dose adjustment)
  • Other antihypertensives (additive hypotensive effect)
  • Alcohol, barbiturates, narcotics (additive orthostatic hypotension)
  • Pressor amines (e.g., norepinephrine) (possible decreased arterial responsiveness)
  • Allopurinol (increased risk of hypersensitivity reactions to allopurinol)
  • Amantadine (increased risk of amantadine toxicity)
  • Calcium salts (increased serum calcium due to decreased excretion)
  • Cyclosporine (increased risk of hyperuricemia and gouty complications)
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Minor Interactions

  • Not available (most clinically significant interactions are moderate or major)

Monitoring

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Baseline Monitoring

Serum Electrolytes (Sodium, Potassium, Magnesium, Calcium)

Rationale: To establish baseline levels and identify pre-existing imbalances, as HCTZ can cause electrolyte disturbances.

Timing: Prior to initiation of therapy.

Renal Function (BUN, Serum Creatinine, eGFR)

Rationale: To assess kidney function, as HCTZ efficacy is reduced in severe renal impairment and it can affect renal perfusion.

Timing: Prior to initiation of therapy.

Blood Pressure

Rationale: To establish baseline and guide initial dosing.

Timing: Prior to initiation of therapy.

Uric Acid

Rationale: HCTZ can increase serum uric acid levels.

Timing: Prior to initiation of therapy.

Blood Glucose

Rationale: HCTZ can cause hyperglycemia, especially in predisposed individuals.

Timing: Prior to initiation of therapy.

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Routine Monitoring

Serum Electrolytes (Sodium, Potassium, Magnesium, Calcium)

Frequency: Periodically, especially during dose titration, intercurrent illness, or with concomitant medications affecting electrolytes. Typically every 1-3 months initially, then every 6-12 months.

Target: Sodium: 135-145 mEq/L; Potassium: 3.5-5.0 mEq/L; Magnesium: 1.7-2.2 mg/dL; Calcium: 8.5-10.5 mg/dL

Action Threshold: Potassium < 3.5 mEq/L (consider supplementation); Sodium < 130 mEq/L (evaluate fluid status); Calcium > 10.5 mg/dL (investigate cause).

Renal Function (BUN, Serum Creatinine)

Frequency: Periodically, especially in elderly or those with pre-existing renal impairment. Typically every 6-12 months.

Target: Within normal limits for age/sex.

Action Threshold: Significant increase in BUN/Creatinine (evaluate for acute kidney injury or worsening renal function).

Blood Pressure

Frequency: Regularly, at each clinic visit or as directed by physician.

Target: Individualized target (e.g., <130/80 mmHg for most adults with hypertension).

Action Threshold: Failure to achieve target BP, or symptomatic hypotension.

Uric Acid

Frequency: Periodically, especially if patient develops symptoms of gout.

Target: Within normal limits (e.g., 3.5-7.2 mg/dL for men, 2.6-6.0 mg/dL for women).

Action Threshold: Elevated levels with symptoms of gout (consider allopurinol or alternative diuretic).

Blood Glucose

Frequency: Periodically, especially in diabetic or pre-diabetic patients.

Target: Fasting: <100 mg/dL; HbA1c: <7% for most diabetics.

Action Threshold: Significant increase in blood glucose (consider adjustment of antidiabetic therapy or alternative antihypertensive).

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Symptom Monitoring

  • Dizziness or lightheadedness (especially upon standing, indicative of hypotension)
  • Muscle cramps or weakness (indicative of hypokalemia or hypomagnesemia)
  • Excessive thirst, dry mouth, lethargy, confusion (indicative of dehydration or hyponatremia)
  • Nausea, vomiting, loss of appetite
  • Swelling of ankles or feet (if edema is not resolving)
  • Signs of gout (sudden joint pain, swelling, redness)
  • Increased urination (expected, but monitor for excessive fluid loss)
  • Skin rash or increased sensitivity to sunlight (photosensitivity)

Special Patient Groups

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Pregnancy

Generally considered Category B. Not recommended for routine use in healthy pregnant women for edema or hypertension, as it does not prevent pre-eclampsia and may reduce placental perfusion. May be used in specific cases where the benefit outweighs the risk, particularly if other antihypertensives are not effective or tolerated.

Trimester-Specific Risks:

First Trimester: Limited data, but generally considered low risk for teratogenicity.
Second Trimester: Generally considered safe if clinically indicated, but close monitoring for maternal and fetal effects is advised.
Third Trimester: Avoided if possible due to potential for fetal/neonatal jaundice, thrombocytopenia, and other adverse reactions observed in adults.
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Lactation

Excreted in breast milk. Use with caution. May suppress lactation due to fluid loss. Potential for adverse effects in the infant (e.g., electrolyte imbalance, jaundice). Consider alternative agents, especially in preterm infants or during the first month postpartum.

Infant Risk: Low to moderate risk (L3). Monitor infant for dehydration, lethargy, poor feeding, and jaundice.
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Pediatric Use

Use with caution. Dosing is weight-based. Not typically first-line for hypertension in children. More susceptible to electrolyte imbalances. Close monitoring of fluid and electrolytes is crucial.

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Geriatric Use

More sensitive to the effects of diuretics, including hypotension and electrolyte imbalances (especially hypokalemia and hyponatremia). Start with lower doses and titrate slowly. Close monitoring of renal function and electrolytes is essential.

Clinical Information

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Clinical Pearls

  • Hydrochlorothiazide is a first-line agent for essential hypertension, especially in patients who are Black or have a history of stroke.
  • Take in the morning to prevent nocturia (nighttime urination).
  • Can cause photosensitivity; advise patients to use sunscreen and protective clothing.
  • May increase serum uric acid, potentially precipitating gout attacks.
  • Can cause hyperglycemia, requiring careful monitoring in diabetic patients.
  • Often used in combination with ACE inhibitors or ARBs to enhance antihypertensive effect and mitigate potassium loss (ACEIs/ARBs tend to increase potassium, while HCTZ decreases it).
  • Ineffective in severe renal impairment (CrCl < 30 mL/min); loop diuretics are preferred in these cases.
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Alternative Therapies

  • Other thiazide diuretics (e.g., Chlorthalidone, Indapamide)
  • Loop diuretics (e.g., Furosemide, Torsemide) for more potent diuresis or renal impairment
  • Potassium-sparing diuretics (e.g., Spironolactone, Amiloride)
  • ACE inhibitors (e.g., Lisinopril, Enalapril)
  • Angiotensin Receptor Blockers (ARBs) (e.g., Valsartan, Losartan)
  • Calcium Channel Blockers (e.g., Amlodipine, Diltiazem)
  • Beta-blockers (e.g., Metoprolol, Atenolol)
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Cost & Coverage

Average Cost: $5 - $20 per 30 tablets (25mg)
Generic Available: Yes
Insurance Coverage: Tier 1 (Preferred Generic) on most formularies due to low cost and widespread use.
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General Drug Facts

If your symptoms or health issues persist or worsen, it's essential to contact your doctor for further guidance. To ensure your safety, never share your medication with others or take someone else's medication. Some medications may come with an additional patient information leaflet, so be sure to check with your pharmacist for more information. If you have any questions or concerns about your medication, don't hesitate to reach out to your doctor, nurse, pharmacist, or other healthcare provider. In the event of a suspected overdose, immediately call your local poison control center or seek medical attention. When reporting the incident, be prepared to provide details about the medication taken, the amount, and the time it occurred.