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What is Naproxene sodico DOC

Naproxene sodico DOC is a nonsteroidal anti-inflammatory drug. Naproxene sodico DOC works by reducing hormones that cause inflammation and pain in the body.
Naproxene sodico DOC is used to treat pain or inflammation caused by conditions such as arthritis, ankylosing spondylitis, tendinitis, bursitis, gout, or menstrual cramps.
Naproxene sodico DOC may also be used for purposes not listed in Naproxene sodico DOC guide.

Naproxene sodico DOC side effects

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.
Stop using Naproxene sodico DOC and call your doctor at once if you have:

Common side effects may include:

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
See also: Side effects (in more detail)
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Naproxene sodico DOC dosing

Usual Adult Dose for Ankylosing Spondylitis:

Initial: 250 mg to 500 mg or 275 mg to 550 mg (naproxen sodium) orally twice a day. The initial dose for Naproxene sodico DOC sodium controlled-release is two 375 mg tablets (750 mg) orally once a day, one 750 mg tablet orally once a day, or two 500 mg tablets (1000 mg) orally once a day.
Maintenance: May be increased to a daily maximum of 1500 mg (naproxen) or 1650 mg (naproxen sodium) in 2 divided doses, for limited periods up to 6 months. In patients who tolerate lower doses well, the dose of Naproxene sodico DOC sodium controlled-release may be increased to two 750 mg tablets (1500 mg) or three 500 mg tablets (1500 mg) orally once a day for limited periods.

Usual Adult Dose for Osteoarthritis:

Initial: 250 mg to 500 mg (naproxen) or 275 mg to 550 mg (naproxen sodium) orally twice a day. The initial dose for Naproxene sodico DOC sodium controlled-release is two 375 mg tablets (750 mg) orally once a day, one 750 mg tablet orally once a day, or two 500 mg tablets (1000 mg) orally once a day.
Maintenance: May be increased to a daily maximum of 1500 mg (naproxen) or 1650 mg (naproxen sodium) in 2 divided doses, for limited periods up to 6 months. In patients who tolerate lower doses well, the dose of Naproxene sodico DOC sodium controlled-release may be increased to two 750 mg tablets (1500 mg) or three 500 mg tablets (1500 mg) orally once a day for limited periods.

Usual Adult Dose for Rheumatoid Arthritis:

Initial: 250 mg to 500 mg or 275 mg to 550 mg (naproxen sodium) orally twice a day. The initial dose for Naproxene sodico DOC sodium controlled-release is two 375 mg tablets (750 mg) orally once a day, one 750 mg tablet orally once a day, or two 500 mg tablets (1000 mg) orally once a day.
Maintenance: May be increased to a daily maximum of 1500 mg (naproxen) or 1650 mg (naproxen sodium) in 2 divided doses, for limited periods up to 6 months. In patients who tolerate lower doses well, the dose of Naproxene sodico DOC sodium controlled-release may be increased to two 750 mg tablets (1500 mg) or three 500 mg tablets (1500 mg) orally once a day for limited periods.

Usual Adult Dose for Acute Gout:

750 mg (naproxen) or 825 mg (naproxen sodium) orally one time, followed by 250 mg (naproxen) or 275 mg (naproxen sodium) every 8 hours until the gouty attack has resolved, usually 2 to 3 days. The recommended dose of Naproxene sodico DOC sodium controlled-release is two to three 500 mg tablets (1000 to 1500 mg) orally on the first day, followed by two 500 mg tablets (1000 mg) orally daily until the attack has subsided.

Usual Adult Dose for Bursitis:

550 mg Naproxene sodico DOC sodium orally once, followed by 550 mg Naproxene sodico DOC sodium every 12 hours, or 275 mg /250 mg (naproxen) every 6 to 8 hours as needed. Titrate to a maximum daily dose of 1100 mg Naproxene sodico DOC sodium or 1000 mg Naproxene sodico DOC. The recommended initial dose of Naproxene sodico DOC sodium controlled-release is two 500 mg tablets (1000 mg) orally once a day. For patients requiring greater analgesic benefit, two 750 mg tablets (1500 mg) or three 500 mg tablets (1500 mg) may be used for a limited period. Thereafter, the total daily dose should not exceed two 500 mg tablets (1000 mg).

Usual Adult Dose for Tendonitis:

550 mg Naproxene sodico DOC sodium orally once, followed by 550 mg Naproxene sodico DOC sodium every 12 hours, or 275 mg (naproxen sodium)/250 mg (naproxen) every 6 to 8 hours as needed. Titrate to a maximum daily dose of 1100 mg Naproxene sodico DOC sodium or 1000 mg Naproxene sodico DOC. The recommended initial dose of Naproxene sodico DOC sodium controlled-release is two 500 mg tablets (1000 mg) orally once a day. For patients requiring greater analgesic benefit, two 750 mg tablets (1500 mg) or three 500 mg tablets (1500 mg) may be used for a limited period. Thereafter, the total daily dose should not exceed two 500 mg tablets (1000 mg).

Usual Adult Dose for Dysmenorrhea:

550 mg Naproxene sodico DOC sodium orally once, followed by 550 mg Naproxene sodico DOC sodium every 12 hours, or 275 mg /250 mg (naproxen) every 6 to 8 hours as needed. Titrate to a maximum daily dose of 1100 mg Naproxene sodico DOC sodium or 1000 mg Naproxene sodico DOC.
Over-the-counter preparation: Naproxene sodico DOC sodium 220 mg orally every 8 hours as needed. Do not exceed 2 caplets in any 8- to 12-hour period.
The recommended initial dose of Naproxene sodico DOC sodium controlled-release is two 500 mg tablets (1000 mg) orally once a day. For patients requiring greater analgesic benefit, two 750 mg tablets (1500 mg) or three 500 mg tablets (1500 mg) may be used for a limited period. Thereafter, the total daily dose should not exceed two 500 mg tablets (1000 mg).

Usual Adult Dose for Pain:

550 mg Naproxene sodico DOC sodium orally once, followed by 550 mg Naproxene sodico DOC sodium every 12 hours, or 275 mg (naproxen sodium)/250 mg (naproxen) every 6 to 8 hours as needed. Titrate to a maximum daily dose of 1100 mg Naproxene sodico DOC sodium or 1000 mg Naproxene sodico DOC.
Over-the-counter preparation: Naproxene sodico DOC sodium 220 mg orally every 8 hours as needed. Do not exceed 2 caplets in any 8- to 12-hour period.
The recommended initial dose of Naproxene sodico DOC sodium controlled-release is two 500 mg tablets (1000 mg) orally once a day. For patients requiring greater analgesic benefit, two 750 mg tablets (1500 mg) or three 500 mg tablets (1500 mg) may be used for a limited period. Thereafter, the total daily dose should not exceed two 500 mg tablets (1000 mg).

Usual Geriatric Dose for Pain:

Over-the-counter preparation - 220 mg orally every 12 hours or 250 mg (naproxen) orally every 8 hours as needed.

Usual Pediatric Dose for Fever:

Dosage guidelines are based on Naproxene sodico DOC:
Greater than 2 years: 2.5 to 10 mg/kg/dose. Maximum daily dose is 10 mg/kg, given every 8 to 12 hours.

Usual Pediatric Dose for Pain:

Dosage guidelines are based on Naproxene sodico DOC:
Greater than 2 years: 2.5 to 10 mg/kg/dose. Maximum daily dose is 10 mg/kg, given every 8 to 12 hours.

Usual Pediatric Dose for Juvenile Rheumatoid Arthritis:

Dosage guidelines are based on Naproxene sodico DOC:
Greater than or equal to 2 years: 5 mg/kg orally twice a day. Maximum dose: 1000 mg/day.

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References

  1. Dailymed."Naproxen: dailymed provides trustworthy information about marketed drugs in the united states. dailymed is the official provider of fda label information (package inserts).". https://dailymed.nlm.nih.gov/dailym... (accessed August 28, 2018).
  2. "Naproxen". https://pubchem.ncbi.nlm.nih.gov/co... (accessed August 28, 2018).
  3. "Naproxen". http://www.drugbank.ca/drugs/DB0078... (accessed August 28, 2018).

Naproxene sodico DOC - Frequently asked Questions

Can Naproxene sodico DOC be stopped immediately or do I have to stop the consumption gradually to ween off?

In some cases, it always advisable to stop the intake of some medicines gradually because of the rebound effect of the medicine.

It's wise to get in touch with your doctor as a professional advice is needed in this case regarding your health, medications and further recommendation to give you a stable health condition.

Who should not take Naproxene sodico DOC?

Naproxene sodico DOC may increase your risk of heart attack or stroke, especially if you use it long term or have heart disease. Do not use this medicine just before or after heart bypass surgery.

Naproxene sodico DOC may also cause stomach or intestinal bleeding, which can be fatal. These conditions can occur without warning while you are taking Naproxene sodico DOC.

You should not use Naproxene sodico DOC if you are allergic to it, or if you have a history of allergic reaction to aspirin or other NSAIDs.

Ask a doctor or pharmacist if it is safe for you to take this medicine if you have:

FDA pregnancy category C. Before using Naproxene sodico DOC, tell your doctor if you are pregnant or plan to become pregnant during treatment. Taking Naproxene sodico DOC during the last 3 months of pregnancy may result in birth defects. Do not take Naproxene sodico DOC during pregnancy unless your doctor has told you to.

Naproxene sodico DOC can pass into breast milk and may harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

Do not give this medicine to a child younger than 2 years old without medical advice.

What other drugs will affect Naproxene sodico DOC?

Ask your doctor before using Naproxene sodico DOC if you take an antidepressant such as citalopram, escitalopram, fluoxetine (Prozac), fluvoxamine, paroxetine, sertraline (Zoloft), trazodone, or vilazodone. Taking any of these medicines with an NSAID may cause you to bruise or bleed easily.

Ask a doctor or pharmacist if it is safe for you to use Naproxene sodico DOC if you are also using any of the following drugs:

This list is not complete. Other drugs may interact with Naproxene sodico DOC, including prescription and over-the-counter medicines, vitamins, and herbal products. Not all possible interactions are listed in this medication guide.

How should I take Naproxene sodico DOC?

Use exactly as directed on the label, or as prescribed by your doctor. Do not use in larger or smaller amounts or for longer than recommended.

The delayed-release tablet is a slower-acting form of Naproxene sodico DOC and should be used only for treating arthritis or ankylosing spondylitis. Follow your doctor's instructions.

Do not crush, chew, or break an extended-release or enteric-coated tablet. Swallow the pill whole. The extended-release pill is specially made to release medicine slowly in the body. The enteric-coated pill has a special coating to protect your stomach.

Shake the oral suspension (liquid) well just before you measure a dose. Measure the liquid with a special dose-measuring spoon or medicine cup. If you do not have a dose-measuring device, ask your pharmacist for one.

If you use this medication long-term, you may need frequent medical tests at your doctor's office.

Store at room temperature away from moisture and heat.

Can Naproxene sodico DOC be taken or consumed while pregnant?

Please visit your doctor for a recommendation as such case requires special attention.

Can Naproxene sodico DOC be taken for nursing mothers or during breastfeeding?

Kindly explain your state and condition to your doctor and seek medical advice from an expert.

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Reviews

Following the study conducted by gmedication.com on Naproxene sodico DOC, the result is highlighted below. However, it must be clearly stated that the survey and result is based solely on the perception and impression of visitors and users of the website as well as consumers of Naproxene sodico DOC. We, therefore, urge readers not to base their medical judgment strictly on the result of this study but on test/diagnosis duly conducted by a certified medical practitioners or physician.

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The information was verified by Dr. Vishal Pawar, MD Pharmacology