Procone

Procone Uses, Dosage, Side Effects, Food Interaction and all others data.

Procone Sodium is an antiulcerant drug in the class of Proton Pump Inhibitors. Procone Sodium is a substituted benzimidazole which suppresses gastric acid secretion by inhibiting the gastric H+/K+-ATPase enzyme at the secretory surface of the gastric parietal cell. It is an enteric coated tablet, because of its coated formulation it is highly stable in stomach and because of higher pKa value of Procone Sodium it provides faster onset of action. It blocks the final step of gastric acid secretion.

After oral administration of 20 mg, Procone is absorbed and can be detected in plasma by 1 hour. The effects of food on the absorption of Procone have not been evaluated. Procone is 96.3% bound to human plasma proteins. Procone is primarily metabolized in the liver by Cytochrome P-450 3A (Sulphone metabolite) and 2C19 (Desmethyl Procone). Following a single 20 mg oral dose of Procone, approximately 90% of the drug is eliminated in the urine.The remainder of the dose is excreted in the feaces.

Procone prevents the production of acid in the stomach. It reduces symptoms and prevents injury to the esophagus or stomach in patients with gastroesophageal reflux disease (GERD) or ulcers. Procone is also useful in conditions that produce too much stomach acid such as Zollinger-Ellison syndrome. Procone may also be used with antibiotics to get rid of bacteria that are associated with some ulcers. Procone is a selective and irreversible proton pump inhibitor, suppresses gastric acid secretion by specific inhibition of the H+, K+ -ATPase, which is found at the secretory surface of parietal cells. In doing so, it inhibits the final transport of hydrogen ions (via exchange with potassium ions) into the gastric lumen.

Trade Name Procone
Availability Prescription only
Generic Rabeprazole
Rabeprazole Other Names Clofezone, Rabeprazole
Related Drugs amoxicillin, omeprazole, famotidine, pantoprazole, metronidazole, Nexium, Pepcid, Protonix, esomeprazole, sucralfate
Weight 20mg
Type Tablet
Formula C18H21N3O3S
Weight Average: 359.443
Monoisotopic: 359.130362243
Protein binding

96.3% (bound to human plasma proteins)

Groups Approved, Investigational
Therapeutic Class Proton Pump Inhibitor
Manufacturer Pharma Health Pakistan (pvt) Ltd
Available Country Pakistan
Last Updated: September 19, 2023 at 7:00 am
Procone
Procone

Uses

Short-term treatment in healing and symptomatic relief of duodenal ulcers and erosive or ulcerative Gastroesophageal Reflux Disease (GERD).

Maintaining healing and reducing relapse rates of heartburn symptoms in patients with GERD.

Treatment of daytime and night time heartburn and other symptoms associated with GERD.

Long-term treatment of pathological hypersecretory conditions, including Zollinger Ellison Syndrome.

In combination with Amoxicillin and Clarithromycin to eradicate Helicobacter pylori.

Procone is also used to associated treatment for these conditions: Duodenal Ulcer, Gastric Ulcer, Gastro-esophageal Reflux Disease (GERD), Heartburn, Helicobacter Pylori Infection, NSAID Associated Gastric Ulcers, Non-erosive Reflux Esophagitis Disease (NERD), Vomiting, Zollinger-Ellison Syndrome, Erosive reflux esophagitis

How Procone works

Procone belongs to a class of antisecretory compounds (substituted benzimidazole proton-pump inhibitors) that do not exhibit anticholinergic or histamine H2-receptor antagonist properties, but suppress gastric acid secretion by inhibiting the gastric H+/K+ATPase (hydrogen-potassium adenosine triphosphatase) at the secretory surface of the gastric parietal cell. Because this enzyme is regarded as the acid (proton) pump within the parietal cell, rabeprazole has been characterized as a gastric proton-pump inhibitor. Procone blocks the final step of gastric acid secretion. In gastric parietal cells, rabeprazole is protonated, accumulates, and is transformed to an active sulfenamide. When studied in vitro, rabeprazole is chemically activated at pH 1.2 with a half-life of 78 seconds.

Dosage

Procone dosage

Healing of Erosive or Ulcerative Gastroesophageal Reflux Disease (GERD): 20 mg to be taken once daily for 4 to 8 weeks. For those patients who have not healed after 8 weeks of treatment, an additional 8 week course may be considered.

Maintenance of Healing of Erosive or Ulcerative Gastroesophageal Reflux Disease (GERD Maintenance): The recommended adult oral dose is 20 mg once daily.

Treatment of Symptomatic Gastroesophageal Reflux Disease (GERD):The recommended adult oral dose is 20 mg once daily for 4 weeks. If symptoms do not resolve completely after 4 weeks, an additional course of treatment may be considered.

Healing of Duodenal Ulcers:The recommended adult oral dose is 20 mg once daily after the morning meal for a period up to four weeks. Most patients with duodenal ulcer heal within four weeks. A few patients may require additional therapy to achieve healing.

Helicobacter pylori Eradication:To Reduce the Risk of Duodenal Ulcer Recurrence-

  • Procone Sodium 20 mg Twice Daily for 7 Days
  • Amoxicillin 1000 mg Twice Daily for 7 Days
  • Clarithromycin 500 mg Twice Daily for 7 Days

All three medications should be taken twice daily with the morning and evening meals. It is important that patients comply with the full 7-day regimen.

Treatment of Pathological Hypersecretory Conditions Including Zollinger-Ellison Syndrome: The dosage of Procone Sodium in patients with pathologic hypersecretory conditions varies with the individual patient. The recommended adult oral starting dose is 60 mg once a day. Doses should be adjusted to individual patient needs and should continue for as long as clinically indicated. Some patients may require divided doses. Doses up to 100 mg QD and 60 mg BID have been administered. Some patients with Zollinger-Ellision syndrome have been treated continuously with Procone Sodium for up to one year.

Side Effects

Procone Sodium may sometimes cause headache, diarrhoea, abdominal pain, vomiting, constipation, dry mouth, increased or decreased appetite, muscle pain, drowsiness and dizziness.

Precaution

Administration of Procone Sodium to patients with mild to moderate liver impairment resulted in increased exposure and decreased elimination. Caution should be exercised in patients with severe hepatic impairment.

Interaction

Procone is metabolized by the Cytochrome P-450 (CYP-450) drug metabolizing enzyme system. Procone does not have clinically significant interactions with other drugs metabolized by the CYP-450 system,such as Warfarin and Theophylline given as single oral dose, Diazepam as a single intravenous dose, and Phenytoin given as a single intravenous dose. In normal subjects, co-administration of Procone 20 mg QD resulted in an approximately 30% decrease in the bioavailability of Ketoconazole and increase in the AUC and Cmax for digoxin of 90% and 29% respectively.

Food Interaction

  • Take with or without food. Food delays drug absorption, but not to a clinically significant extent.

Elimination Route

Absolute bioavailability is approximately 52%.

Half Life

1-2 hours (in plasma)

Elimination Route

Following a single 20 mg oral dose of 14C-labeled rabeprazole, approximately 90% of the drug was eliminated in the urine, primarily as thioether carboxylic acid; its glucuronide, and mercapturic acid metabolites.

Pregnancy & Breastfeeding use

Procone is FDA Pregnancy Category B. No data is available on administration of Procone to pregnant women. However this drug should be used during pregnancy, only if clearly needed. There are no data on the excretion of Procone into the breast milk. A decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the benefit of the drug to the mother.

Contraindication

Procone Sodium is contraindicated in patient with known hypersensitivity to Procone or to any component in the product.

Special Warning

Use in pediatric patients: The safety and effectiveness of Procone in pediatric patients have not been established.

Acute Overdose

There has been no experience with large overdoses with Procone. No specific antidote for Procone is known. Procone is extensively protein bound and is not readily dialyzable. In the event of overdosage, treatment should be symptomatic and supportive.

Storage Condition

Store below 25°C, protected from light and moisture. Keep all medicines out of the reach of the children.

Innovators Monograph

You find simplified version here Procone

Procone contains Rabeprazole see full prescribing information from innovator Procone Monograph, Procone MSDS, Procone FDA label

FAQ

What is Procone used for?

Procone used for heartburn, acid reflux and gastro-oesophageal reflux disease when you keep getting acid reflux. Procone is also taken to prevent and treat stomach ulcers. Procone reduces the amount of acid your stomach makes.

How safe is Procone?

Procone is efficacious in gastro-esophageal reflux disease (GERD) and other acid-related diseases. Long-term use of Procone was confirmed to be safe in studies of two to five-year maintenance therapy for GERD.

What are side effects of Procone?

Common side effects may include:

  • infection;
  • pain;
  • sore throat;
  • headache;
  • nausea, vomiting;
  • gas, diarrhea, constipation; or.
  • stomach pain.

Is Procone taken empty stomach?

Procone can be taken either before or after food, although taking it before food is preferable. If you forget to take a dose at your usual time, you can generally take it when you remember.

Is Procone safe for my kidneys?

Procone can cause kidney problems.If you have blood in your urine. Diarrhea may be a sign of a new infection.

Is Procone safe during pregnancy?

Procone isn't usually recommended during pregnancy as there's no firm evidence it's safe. if you're pregnant, it's better to try to treat symptoms of acid reflux and heartburn without taking a medicine.

Is Procone safe to take while breastfeeding?

The SPC advises to avoid the use of rabeprazole during lactation.levels for both drugs are low, and in addition a large proportion of any of the drug ingested by the infant is likely to be destroyed by the acid in the stomach.

Does Procone work right away?

Procone starts doing its job within an hour of taking the first dose, you may not feel that your symptoms have improved for several days. This is because Procone has to “turn off” the proton pumps of the acid-producing cells in the stomach, and it is not able to turn off all proton pumps immediately.

How long Procone can be taken?

Procone is for short-term use only, usually 4 to 8 weeks. Your doctor may recommend a second course of treatment if you need additional healing time.

Is Procone good for gastritis?

Procone may good to treat: Reflux oesophagitis. Peptic ulcers. Chronic Gastritis.

Can Procone cause liver problems?

Procone therapy is associated with a low rate of transient and asymptomatic serum aminotransferase elevations and is a rare cause of clinically apparent liver injury.

Is Procone safe long term?

The drug is efficacious in gastro-esophageal reflux disease (GERD) and other acid-related diseases. Long-term use of Procone was confirmed to be safe in studies of two to five-year maintenance therapy for GERD.

What happens when you stop taking Procone?

Stopping the Procone suddenly could make your stomach produce a lot more acid, and make your symptoms return.you can stop taking rabeprazole without reducing the dose first. If you've taken Procone for a long time, speak to your doctor before you stop taking Procone.

Is Procone an antifungal?

Proton pump inhibitors, such as Procone act as agents with antifungal activity or reverse-acquired resistance to azoles.

Is Procone a controlled substance?

Procone 20 mg is not a controlled substance under the Controlled Substances Act (CSA).

What class of drug is Procone?

Procone is in a class of medications called proton-pump inhibitors.

Can you take Tylenol with Procone?

No interactions were found between Procone and Tylenol. This does not necessarily mean no interactions exist. Always consult your healthcare provider.

How many Procone Can I take a day?

Adults can take Procone 20 milligrams (mg) once a day for up to 4 weeks. Your doctor may adjust your dose as needed. Children 12 years of age and older take Procone 20 mg once a day for up to 8 weeks. Your child's doctor may adjust the dose as needed.

*** Taking medicines without doctor's advice can cause long-term problems.
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