Eva Q
Eva Q Uses, Dosage, Side Effects, Food Interaction and all others data.
A fungistatic compound that is widely used as a food preservative. It is conjugated to GLYCINE in the liver and excreted as hippuric acid. As the sodium salt form, sodium benzoate is used as a treatment for urea cycle disorders due to its ability to bind amino acids. This leads to excretion of these amino acids and a decrease in ammonia levels. Recent research shows that sodium benzoate may be beneficial as an add-on therapy (1 gram/day) in schizophrenia. Total Positive and Negative Syndrome Scale scores dropped by 21% compared to placebo.
In the colon it is broken down to short chain organic acids and increases osmotic pressure in the colon, thereby causing an increase in the stool water content and stool volume.
Lactitol helps to facilitate bowel movements by drawing water into the gastrointestinal tract. The oral administration of lactitol may reduce the absorption of concomitant medications - other oral medications should be administered at least 2 hours before or 2 hours after lactitol.
Trade Name | Eva Q |
Generic | Lactitol + Benzoic Acid |
Weight | 3.33g |
Type | Syrup |
Therapeutic Class | |
Manufacturer | Medley Pharmaceutical Pvt Ltd |
Available Country | India |
Last Updated: | September 19, 2023 at 7:00 am |
Uses
Benzoic acid is an antimicrobial food additive.
Constipation, Hepatic encephalopathy
Eva Q is also used to associated treatment for these conditions: Infections, Fungal, Oropharyngeal pain, Pain, Ringworm, Sore Throat, Tinea Pedis, Burning sensation in the mouth, Dry cough, Mouth infection, Throat infectionsConstipation, Hepatic Encephalopathy (HE), Occasional Constipation, Chronic idiopathic constipation (CIC)
How Eva Q works
Lactitol is an osmotic laxative - it exerts its pharmacologic effect by creating a hyperosmotic environment within the small intestine. The osmotic effect generated by lactitol draws water into the small intestine, which loosens stools and ultimately facilitates bowel movements.
Dosage
Eva Q dosage
2 teaspoonfuls (20 gm) once or twice daily with plenty of water
Side Effects
Abdominal distension, flatulance and abdominal cramp.
Toxicity
The LD50 is 23 g/kg in mice and >30 g/kg in rats.
Experience with acute overdosage is limited, but is likely to involve significant gastrointestinal upset and diarrhea consistent with the pharmacologic profile of lactitol. Overdosage should be managed with symptomatic and supportive measures, where necessary.
Precaution
Lactose intolerance.
Volume of Distribution
Data regarding the volume of distribution of lactitol are unavailable.
Elimination Route
In healthy subjects under fed conditions, oral administration of 20 grams of lactitol resulted in a mean Tmax of 3.6 ± 1.2 hours, Cmax of 776 ± 253 ng/mL, and a mean AUC of 6,019 ± 1,771 ng*hr/mL.
Half Life
The average half-life of orally administered lactitol is 2.4 hours.
Clearance
Data regarding the clearance of lactitol are unavailable.
Elimination Route
Lactitol is not absorbed in the gastrointestinal tract to any significant extent. The vast majority of an ingested dose is likely degraded into organic acids in the colon and eliminated in the feces.
Pregnancy & Breastfeeding use
Pregnancy Category - Not Classified. FDA has not yet classified the drug into a specified pregnancy category.
Contraindication
Patients with known hypersensitivity to any of the active substance. Gastro-intestinal obstruction. Galactosaemia.
Innovators Monograph
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