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Common side effects of senna glycoside include abdominal cramps. [3] It is not recommended for long-term use, as it may result in poor bowel function or electrolyte problems. [1] While no harm has been found to result from use while breastfeeding, such use is not typically recommended. [1] It is not typically recommended in children. [1]
"rare and mild gastrointestinal upset, headaches, diarrhea, gynecomastia, paroxysmal atrial fibrillation, ventricular rupture and death in one patient" [3] Senna: Egyptian senna Senna alexandrina (Cassia senna) "abdominal pain, diarrhea, potentially carcinogenic, with others can potentiate cardiac glycosides and antiarrhythmic agents", [3 ...
Once the bark is dry, and the specially made calabash gourd, or Sotet, has been cleaned and dried, the senna bark is put in a fire, and removed when charred. The process emits fragrant smoke. The charred bark is used to coat the inside of the gourd, which is subsequently used for the storage of fermented or fresh milk. [8]
Here's What 'Diarrhea' Actually Means and When You Should Worry About It, According to Gastroenterologists. Erica Sweeney. August 10, 2023 at 5:59 AM ... can offer short-term relief. But, don’t ...
Used as an anti-inflammatory [23] and for osteoarthritis. [24] The US Food and Drug Administration has classified Arnica montana as an unsafe herb because of its toxicity. [25] It should not be taken orally or applied to broken skin where absorption can occur. [25] Astragalus propinquus: Astragalus: Long used in traditional Chinese medicine. [26]
Historically, Senna alexandrina was used in the form of senna pods, or as herbal tea made from the leaves, as a laxative. [6] It also serves as a fungicide. [6] Modern medicine has used senna extracts since at least the 1950s [7] as a laxative. [8] [9] If accidentally ingested by infants, it can cause side effects such as severe diaper rash. [8]
Drugs such as morphine or codeine can be used to relieve diarrhoea this way. A notable opioid for the purpose of relief of diarrhoea is loperamide which is only an agonist of the μ opioid receptors in the large intestine and does not have opioid affects in the central nervous system as it doesn't cross the blood–brain barrier in significant ...
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