Medication info
Daewoong Bio Propiverine Tablets 20 mg (Propiverine Hydrochloride)

Daewoong Bio Propiverine Tablets 20 mg (Propiverine Hydrochloride)

Prescription medicationTabletOral
Ingredient · strength
Propiverine Hydrochloride›20mg / 1 tablet
Manufacturer / importer
Daewoong Bio Co., Ltd.
Appearance
White round film-coated tablets
Packaging
30 tablets/bottle, 100 tablets/bottle
Approval status
Active

MFDS item code 200501390 · Approved 2005.11.23 · Insurance code 694000510

Summary

Main use
Relief of symptoms of overactive bladder (urgency, etc.) and urinary frequency and incontinence associated with neurogenic bladder
Who takes it
Adults
Adult dose
Adults: Administer propiverine hydrochloride 20 mg orally once daily after a meal. The dose may be adjusted according to symptoms; if the effect is inadequate and there are no safety concerns, 20 mg may be taken up to twice daily.

Ingredients

Manufacturer
Daewoong Bio Co., Ltd.

Efficacy & effects

Relief of symptoms of overactive bladder (urgency, etc.) and urinary frequency and incontinence associated with neurogenic bladder

  • Frequent urination
  • urinary incontinence
  • neurogenic bladder
  • neurogenic frequent urination
  • unstable bladder
  • bladder irritation
  • chronic cystitis
  • chronic prostatitis
  • urinary urgency
  • urge urinary incontinence
View approved original text

This medication is used to treat frequent urination and urinary incontinence caused by the following conditions or diseases. The main indications include neurogenic bladder, neurogenic frequent urination, unstable bladder, chronic cystitis, and chronic prostatitis, which are conditions that irritate the bladder. It is also effective for the treatment of urinary urgency, frequent urination, and urge urinary incontinence caused by overactive bladder. Therefore, this medication helps regulate bladder function and improve symptoms.

How to take

Adult dose

Adults: Administer propiverine hydrochloride 20 mg orally once daily after a meal. The dose may be adjusted according to symptoms; if the effect is inadequate and there are no safety concerns, 20 mg may be taken up to twice daily.

Precautions

This medication should not be used in certain patients. Patients with an allergy to this medication or its components should not take it. Patients with gastrointestinal obstruction or poor motility may experience worsening of symptoms due to this medication and should avoid using it. Patients with decreased muscle function of the gastrointestinal tract may also experience worsening of symptoms due to this medication. Caution is advised for patients who have difficulty urinating as bladder function may decrease and symptoms may worsen. Patients with angle-closure glaucoma should not take this medication, and other glaucoma patients should use it cautiously. Patients with myasthenia gravis may experience worsening of symptoms due to this medication. Patients with severe heart disease should avoid using this medication as side effects may worsen symptoms. Patients with toxic megacolon or ulcerative colitis may also find this medication to be risky. Patients with moderate to severe liver dysfunction should use this medication cautiously. Patients with a history of arrhythmias should be cautious due to the risk of cardiac side effects. Additionally, this medication contains lactose, so it should not be used by patients with lactose intolerance or certain genetic metabolic disorders. Caution should be exercised when administering this medication to patients with specific diseases such as dysuria, liver dysfunction, kidney dysfunction, symptoms of Parkinson's disease, hyperthyroidism, the elderly, autonomic neuropathy, coronary artery disease, congestive heart failure, and glaucoma. Serious side effects such as hallucinations, delirium, severe constipation, abdominal bloating, irregular heartbeat, thrombocytopenia, renal impairment, skin rash, eye pain due to elevated intraocular pressure, liver dysfunction, muscle pain, and rhabdomyolysis may occur during the use of this medication. Patients should consult their doctor immediately if they experience any abnormal symptoms. Additionally, drowsiness, dizziness, and blurred vision may occur, so driving or operating hazardous machinery should be avoided. This medication may have an increased risk of side effects when taken with anticholinergics, tricyclic antidepressants, phenothiazine medications, and MAO inhibitors, so it is important to inform the doctor. Women who are pregnant or may become pregnant are advised not to use this medication, and breastfeeding women should also discontinue breastfeeding while using this medication. The safety of this medication in pediatric patients has not been established, so it is recommended not to use it in children. The elderly may have decreased liver and kidney function, so it should be used carefully starting at a lower dose. In case of overdose, symptoms such as delirium, excitement, convulsions, gait disturbances, urinary disturbances, and cardiac abnormalities may occur, requiring immediate emergency care. This medication should be stored out of the reach of children, and care should be taken not to transfer it to other containers as this may adversely affect quality.

Side effects

  • Hallucinations
  • delusions
  • paralytic ileus
  • constipation
  • abdominal distension
  • palpitations
  • extrasystole
  • bradycardia
  • QT prolongation
  • ventricular tachycardia
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  • heart block
  • thrombocytopenia
  • renal dysfunction
  • urinary retention
  • skin and mucosal syndrome
  • fever
  • erythema
  • itching
  • conjunctival hyperemia
  • stomatitis
  • increased intraocular pressure
  • acute glaucoma attack
  • nausea
  • headache
  • vision impairment
  • liver dysfunction
  • jaundice
  • myalgia
  • weakness
  • increased CK
  • rhabdomyolysis
  • thirst
  • abdominal pain
  • nausea
  • vomiting
  • dyspepsia
  • diarrhea
  • loss of appetite
  • stomatitis
  • glossitis
  • dysuria
  • post-urinary residual
  • loss of urge to urinate
  • dizziness
  • headache
  • numbness
  • drowsiness
  • insomnia
  • tremor
  • consciousness disturbance
  • perceptual disturbance
  • transient amnesia
  • Parkinsonism
  • dyskinesia
  • hypotension
  • hypertension
  • chest pain
  • hypersensitivity
  • itching
  • rash
  • urticaria
  • control disorder
  • dry eye syndrome
  • elevated AST
  • elevated ALT
  • elevated ALP
  • elevated BUN
  • elevated creatinine
  • leukopenia
  • fatigue
  • lethargy
  • edema
  • weakness
  • taste disturbance
  • low back pain
  • hoarseness
  • sputum
  • agitation
  • heat due to decreased sweating
  • weakness
  • pharyngalgia
  • delusions
  • agitation
  • generalized convulsions
  • gait disturbance
  • speech disturbance
  • mydriasis
  • generalized flushing
  • liver disorder

Not everyone experiences these, and they can vary from person to person.

Storage

This medication should be stored in a tightly sealed container to protect it from air and moisture. It is important to maintain a storage temperature between 1 degree and 30 degrees Celsius. Proper storage can help maintain the effectiveness of the medication for a longer period.

Appearance and packaging

Appearance

White round film-coated tablets

Package unit

30 tablets/bottle, 100 tablets/bottle

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.

Questions about this medicine

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This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.