Probanthine (Propantheline) Medication


Probanthine (Propantheline)

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Drug Description


Pro-banthine is an integral component of therapeutic regimens aimed at addressing peptic ulcers. 

Pro-banthine may find application in clinical contexts beyond those explicitly delineated in this medication guide. 

Uses and Dosage 

Compliance with the instructions provided on your prescription label and thorough perusal of all accompanying medication guides or instruction sheets is imperative. Your physician may intermittently modify your prescribed dosage. Adhere precisely to the prescribed regimen. 

Typically, Pro-Banthine is administered 3 to 4 times daily, with each dose taken approximately 30 minutes before meals and at bedtime, following the precise directives furnished by your healthcare professional. 

For proper storage, keep Pro-Banthine at room temperature, ensuring Probanthine is shielded from excessive moisture and heat exposure. 

Side Effects 

Allergic Reaction

Seek immediate medical attention if you experience signs of an allergic reaction, such as hives, difficulty breathing, or swelling of the face, lips, tongue, or throat. 

Severe Side Effects

Discontinue the use of Pro-Banthine and promptly contact your healthcare provider if you encounter any of the following serious side effects: 

  • Diarrhea 
  • Rapid or irregular heartbeats, palpitations, or sensations of fluttering in the chest 
  • Eye pain, redness, or seeing halos around lights 
  • Painful or challenging urination or a noticeable reduction in urination 

Common Side Effects

Common side effects associated with Pro-Banthine may encompass: 

  • Dryness of the mouth, nose, or throat 
  • Blurred vision 
  • Constipation 
  • Headache, dizziness, or drowsiness 
  • Confusion or heightened nervousness 
  • Reduced sweating 
  • Nausea, vomiting, or bloating 
  • Diminished sense of taste 
  • Impotence or sexual difficulties 
  • Sleep disturbances (insomnia) 

Note that this list of side effects is not exhaustive; other adverse reactions may also manifest. 


Pro-banthine should not be administered if you exhibit any of the following conditions or circumstances: 

  • Allergy to Pro-Banthine or its components 
  • The presence of a stomach or bowel obstruction, including paralytic ileus 
  • A diagnosis of glaucoma 
  • Bladder obstruction or any other issues related to urination 
  • Severe constipation 
  • Severe ulcerative colitis or toxic megacolon 
  • Ongoing bleeding accompanied by rapid heartbeats, low blood pressure, shortness of breath, and cold extremities 
  • A history of myasthenia gravis 

Inform your healthcare provider if you have previously experienced: 

  • A nerve-muscle disorder 
  • Heart disease or any heart rhythm irregularities 
  • High blood pressure 
  • An intestinal disorder such as ulcerative colitis 
  • Liver or kidney disease 
  • A hiatal hernia or reflux esophagitis (GERD) 
  • A thyroid disorder 
  • A history of colostomy or ileostomy 

Disclose your pregnancy or breastfeeding status to your doctor, as Pro-Banthine’s safety during pregnancy and lactation should be carefully considered. 

Furthermore, it should be noted that older adults may display heightened sensitivity to the effects of this medication. 

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Quality Prescription Drugs has provided information from third parties intended to increase awareness and does not contain all the information about Probanthine (Propantheline). Talk to your doctor or a qualified medical practitioner for medical attention, advice, or if you have any concerns about Probanthine (Propantheline).