Package Leaflet: Information for the User
Bohm Evacuant Solution Powder for Oral Solution in Sachets
Macrogol 4000, Sodium Chloride, Potassium Chloride, Anhydrous Sodium Sulfate,
Sodium Hydrogen Carbonate, Sodium Phosphate.
Read the entire package leaflet carefully before starting to take this medication, as it contains important information for you.
Contents of the Package Leaflet
Bohm Evacuant Solution belongs to a group of medications called osmotic laxatives that induce intestinal evacuation.
Bohm Evacuant Solution is indicated in adults for:
Do not take Bohm Evacuant Solution:
Warnings and Precautions
Consult your doctor or pharmacist before starting to take Bohm Evacuant Solution.
Children and Adolescents
Its use is not recommended in this population.
Using Bohm Evacuant Solution with Other Medications
Inform your doctor or pharmacist if you are using, have recently used, or may need to use any other medication.
Avoid using other medications when using Bohm Evacuant Solution. Medication administered during the use of Bohm Evacuant Solution or up to one hour after its administration may be eliminated by the gastrointestinal tract and not absorbed.
Pregnancy, Breastfeeding, and Fertility
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist.
As a precaution, it is preferable to avoid the use of Bohm Evacuant Solution during pregnancy.
No effects are expected in children/breastfed infants since the absorption of Bohm Evacuant Solution in breastfeeding mothers is insignificant.
Driving and Using Machines
Bohm Evacuant Solution does not affect the ability to drive or use machines.
Bohm Evacuant Solution Contains Sodium and Potassium
Patients with renal insufficiency or those on low-potassium diets should note that this medication contains 390 mg (9.98 mmol) of potassium per liter of solution.
Patients on low-sodium diets should note that this medication contains 2,950 mg (128.33 mmol) of sodium per liter of solution.
Follow the administration instructions of this medication exactly as indicated by your doctor. In case of doubt, consult your doctor again.
The recommended dose is:
16 sachets, taking 1 sachet dissolved in 200-250 ml of water (a glass) every 10-15 minutes, until the entire volume has been ingested or the stool is clear. Do not eat any food during the 3 or 4 hours before administration and do not eat solid food in the 2 hours before use.
Administration of the solution is done orally, and a nasogastric tube can be used in patients who are reluctant or unable to drink the solution.
The first intestinal movement should occur approximately one hour after starting administration of the solution.
1 or 2 sachets per day, each dissolved in 250 ml (a glass) of water.
In elderly patients, it is recommended to start with 1 sachet per day.
As with all laxatives, prolonged use of Bohm Evacuant Solution is not recommended.
Do not use Bohm Evacuant Solution for more than six days without consulting your doctor.
Instructions for Correct Administration
This medication is administered orally.
To prepare the solution, pour the contents of a sachet into a glass, add water to approximately 250 ml, and shake until the powder is completely dissolved.
Administration through a nasogastric tube will be performed at a rate of 20-30 ml per minute (1.2 to 1.8 liters per hour).
If You Take More Bohm Evacuant Solution Than You Should
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone 915 620 420, indicating the product and quantity ingested.
If You Forget to Take Bohm Evacuant Solution
Do not take a double dose to make up for forgotten doses.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
Like all medications, this medication can cause side effects, although not everyone experiences them.
Frequent side effects (may affect up to 1 in 10 patients) are: Nausea, feeling of abdominal fullness, and abdominal bloating.
Uncommon side effects (may affect up to 1 in 100 patients) are: Abdominal cramps, vomiting, and anal irritation.
These adverse reactions are transient and resolve quickly.
With an unknown frequency (cannot be estimated from available data), urticaria, nasal drip, and skin irritation may appear as a manifestation of an allergic reaction.
Reporting Side Effects
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect not listed in this package leaflet. You can also report them directly through the Spanish Medication Surveillance System for Human Use: https://www.notificaram.es.
By reporting side effects, you can contribute to providing more information on the safety of this medication.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date shown on the packaging after CAD. The expiration date is the last day of the month indicated.
No special storage conditions are required.
Once the solution is prepared, it is recommended to take it immediately.
Medications should not be thrown away through wastewater or household waste. Deposit the packaging and medications you no longer need at the SIGRE point in the pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. This will help protect the environment.
Composition of Bohm Evacuant Solution.
Appearance of the Product and Package Contents
White crystalline powder in individual sachets. Each single-dose sachet contains 17.73 g of product to prepare 250 ml of solution.
The prepared solution is colorless and particle-free.
Each package contains 16 single-dose sachets for preparing 4 liters of solution.
Each clinical package contains 496 single-dose sachets.
Only some package sizes may be marketed.
Marketing Authorization Holder and Manufacturer
LABORATORIOS BOHM, S.A.
C/ Molinaseca 23-25. Polígono Industrial Cobo Calleja.
28947 Fuenlabrada – Madrid (Spain).
Date of the last revision of this package leaflet: October 2020
Detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.es