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Gastroesophageal Reflux Disease (GERD): Itopride helps alleviate symptoms of GERD, such as heartburn and acid reflux, by increasing the motility of the gastrointestinal tract and enhancing gastric emptying.
Functional Dyspepsia: Itopride is commonly prescribed for the treatment of functional dyspepsia, a condition characterized by persistent or recurrent pain or discomfort centered in the upper abdomen, often accompanied by bloating, early satiety, and nausea.
Symptomatic Relief of Dyspeptic Symptoms: Itopride can provide relief from dyspeptic symptoms, including postprandial fullness, bloating, nausea, and epigastric pain.
Enhancement of Gastric Motility: Itopride works by blocking the dopamine D2 receptors and acetylcholinesterase, leading to an increase in acetylcholine levels and stimulation of gastrointestinal motility.
Improvement in Gastric Emptying: By enhancing gastric motility, itopride promotes faster emptying of the stomach contents, which can be beneficial for individuals with delayed gastric emptying.
Treatment of Gastroparesis: Itopride may be used off-label in the treatment of gastroparesis, a condition characterized by delayed gastric emptying, resulting in symptoms such as nausea, vomiting, abdominal pain, and bloating.
Reduction of Gastrointestinal Symptoms: Itopride can help reduce symptoms associated with various gastrointestinal disorders, including abdominal discomfort, distension, and early satiety.
Adjunctive Therapy: Itopride may be used as adjunctive therapy alongside proton pump inhibitors (PPIs) or H2-receptor antagonists in the management of GERD or other acid-related disorders.
Minimal Central Nervous System (CNS) Side Effects: Unlike some other gastrointestinal motility agents, itopride has minimal penetration of the blood-brain barrier, reducing the risk of central nervous system side effects such as extrapyramidal symptoms.
Well-Tolerated: Itopride is generally well-tolerated, with most adverse effects being mild and transient, including diarrhea, headache, abdominal pain, and nausea.
Rank | Probiotic | Impact |
---|---|---|
species | Parabacteroides distasonis | Reduces |
We extend modifiers to include items that changes the parent and child taxa. I.e. for a species, that would be the genus that is belongs to and the strains in the species.
π Direct Citations | πͺπΆ Indirect Citations | Taxonomy | Rank | Effect |
---|---|---|---|---|
0 | 1 | Parabacteroides | genus | Decreases |
0 | 1 | Bilophila | genus | Decreases |
0 | 1 | Segatella | genus | Decreases |
1 | 0 | Bilophila wadsworthia | species | Decreases |
1 | 0 | Parabacteroides distasonis | species | Decreases |
1 | 0 | Segatella copri | species | Decreases |
A higher number indicates impact on more bacteria associated with the condition and confidence on the impact.
We have X bacteria high and Y low reported. We find that the modifier reduces some and increases other of these two groups. We just tally: X|reduces + Y|Increase = Positive X|increases + Y|decrease = Negative.
Benefit Ratio:
Numbers above 0 have increasing positive effect.
Numbers below 0 have increasing negative effect.
Condition | Positive Impact | Negative Impact | Benefit Ratio Impact |
---|---|---|---|
Abdominal Aortic Aneurysm | 0.3 | 0.3 | |
ADHD | 0.4 | 0.4 | |
Age-Related Macular Degeneration and Glaucoma | 0.4 | -0.4 | |
Allergic Rhinitis (Hay Fever) | 0.4 | 0.4 | |
Allergies | 0.4 | 0 | 0 |
Allergy to milk products | 0.4 | -0.4 | |
Alopecia (Hair Loss) | 0.1 | 0.1 | |
Alzheimer's disease | 0.7 | 0.6 | 0.17 |
Ankylosing spondylitis | 0.2 | 0.2 | |
Anorexia Nervosa | 0.4 | 0.4 | |
Antiphospholipid syndrome (APS) | 0.3 | -0.3 | |
Atrial fibrillation | 0.4 | 0.7 | -0.75 |
Autism | 0.5 | 0.9 | -0.8 |
Bipolar Disorder | 0.7 | 0.7 | |
Carcinoma | 0.7 | 0.4 | 0.75 |
Celiac Disease | 0.7 | -0.7 | |
Chronic Fatigue Syndrome | 0.7 | -0.7 | |
Chronic Kidney Disease | 0.4 | 0.3 | 0.33 |
Chronic Urticaria (Hives) | 0 | 0 | |
Coagulation / Micro clot triggering bacteria | 0.4 | 0.4 | |
Cognitive Function | 0.4 | 0.4 | |
Colorectal Cancer | 0.4 | 0.4 | |
COVID-19 | 0.4 | 0 | 0 |
Crohn's Disease | 0.9 | 0.4 | 1.25 |
Depression | 0.9 | 0.4 | 1.25 |
Endometriosis | 0.4 | 0.4 | |
Epilepsy | 0.4 | -0.4 | |
Fibromyalgia | 0.4 | 0 | 0 |
Functional constipation / chronic idiopathic constipation | 0.4 | 0.5 | -0.25 |
gallstone disease (gsd) | 0.4 | 0.4 | |
Graves' disease | 0.4 | 0.4 | |
Hashimoto's thyroiditis | 0.3 | -0.3 | |
Heart Failure | 0.4 | 0.4 | |
hemorrhagic stroke | 0.4 | 0.4 | |
Hidradenitis Suppurativa | 0.3 | 0.3 | |
hyperglycemia | 0.4 | -0.4 | |
Hyperlipidemia (High Blood Fats) | 0.3 | 0.3 | |
hypersomnia | 0.3 | -0.3 | |
hypertension (High Blood Pressure | 0.4 | 0.3 | 0.33 |
Hypoxia | 0.4 | 0 | 0 |
IgA nephropathy (IgAN) | 0.4 | 0 | 0 |
Inflammatory Bowel Disease | 0.4 | 0.8 | -1 |
Intelligence | 0 | 0 | |
Intracranial aneurysms | 0.4 | 0.4 | |
Irritable Bowel Syndrome | 0.4 | -0.4 | |
ischemic stroke | 0.4 | 0.4 | |
Liver Cirrhosis | 0.7 | 0.3 | 1.33 |
Long COVID | 0.4 | 0.7 | -0.75 |
Lung Cancer | 0.3 | 0.3 | |
ME/CFS without IBS | 0.1 | -0.1 | |
Metabolic Syndrome | 1.3 | 0.7 | 0.86 |
Mood Disorders | 0.9 | 0.4 | 1.25 |
Multiple Sclerosis | 0.7 | 0.6 | 0.17 |
neuropathic pain | 0.4 | -0.4 | |
Neuropathy (all types) | 0.4 | -0.4 | |
Nonalcoholic Fatty Liver Disease (nafld) Nonalcoholic | 0 | 0 | |
Obesity | 0.9 | 0.4 | 1.25 |
obsessive-compulsive disorder | 0.4 | 0 | 0 |
Parkinson's Disease | 0.7 | 0 | 0 |
Polycystic ovary syndrome | 0.6 | 0.3 | 1 |
Premenstrual dysphoric disorder | 0.4 | -0.4 | |
Primary sclerosing cholangitis | 0.4 | 0.6 | -0.5 |
Psoriasis | 0.6 | -0.6 | |
rheumatoid arthritis (RA),Spondyloarthritis (SpA) | 0.7 | 0.7 | |
Schizophrenia | 0.7 | 0.4 | 0.75 |
scoliosis | 0.3 | -0.3 | |
Sjögren syndrome | 0.5 | 0.4 | 0.25 |
Stress / posttraumatic stress disorder | 0.4 | 0.4 | 0 |
Systemic Lupus Erythematosus | 0.7 | 0.7 | |
Tic Disorder | 0 | 0 | |
Type 1 Diabetes | 0.3 | 0.3 | |
Type 2 Diabetes | 0.7 | 0.4 | 0.75 |
Ulcerative colitis | 0.4 | 0.7 | -0.75 |
Unhealthy Ageing | 0.3 | 0.4 | -0.33 |
Vitiligo | 0.4 | 0.4 | 0 |
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