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Lancet, The, ISSN 0140-6736, 2010, Volume 376, Issue 9736, pp. 173 - 179
Summary Background Cyclo-oxygenase (COX)-2-selective non-steroidal anti-inflammatory drugs (NSAIDs) and non-selective NSAIDs plus a proton-pump inhibitor (PPI)... 
Internal Medicine | GASTROINTESTINAL TOXICITY | MEDICINE, GENERAL & INTERNAL | MANAGEMENT | NONSTEROIDAL ANTIINFLAMMATORY DRUGS | MUCOSAL INJURY | OARSI RECOMMENDATIONS | RISK | NAPROXEN | PLUS OMEPRAZOLE | KNEE OSTEOARTHRITIS | EVIDENCE-BASED RECOMMENDATIONS | Lower Gastrointestinal Tract - drug effects | Osteoarthritis - ethnology | Humans | Middle Aged | Peptic Ulcer - prevention & control | Male | Osteoarthritis - drug therapy | Cyclooxygenase 2 Inhibitors - adverse effects | Arthritis, Rheumatoid - drug therapy | Adult | Female | Drug Therapy, Combination | Pyrazoles - adverse effects | Anti-Ulcer Agents - therapeutic use | Omeprazole - therapeutic use | Double-Blind Method | Drug Administration Schedule | Risk Assessment | Diclofenac - adverse effects | Risk Factors | Treatment Outcome | Celecoxib | Pyrazoles - administration & dosage | Anti-Inflammatory Agents, Non-Steroidal - adverse effects | Upper Gastrointestinal Tract - drug effects | Arthritis, Rheumatoid - ethnology | Anti-Inflammatory Agents, Non-Steroidal - administration & dosage | Sulfonamides - adverse effects | Diclofenac - administration & dosage | Peptic Ulcer - chemically induced | Research Design | Sulfonamides - administration & dosage | Omeprazole | Rheumatoid arthritis | Dosage and administration | Research | Comparative analysis | Drug therapy | Diclofenac | Heart failure | Likert scale | Inflammatory bowel disease | Arthritis | Clinical medicine
Journal Article
Pharmacology and Therapeutics, ISSN 0163-7258, 2010, Volume 126, Issue 1, pp. 21 - 38
has been used to treat gastrointestinal (GI) conditions that range from enteric infections and inflammatory conditions to disorders of motility, emesis and... 
Obesity | Fatty acid amide hydrolase | Ion transport | CB 2 receptor | Gastric acid secretion | Intestinal motility | Emesis | Anandamide | Inflammatory bowel disease | Enteric nervous system | Colon cancer | CB 1 receptor | Food intake | Irritable bowel syndrome | Visceral sensation | Colitis | receptor | GUINEA-PIG ILEUM | CARDIOMETABOLIC RISK-FACTORS | GLUCAGON-LIKE PEPTIDE-1 | LOWER ESOPHAGEAL SPHINCTER | PHARMACOLOGY & PHARMACY | CB2 receptor | LITHIUM-PAIRED CONTEXT | VANILLOID RECEPTOR VR1 | COLORECTAL-CARCINOMA CELLS | CB1 receptor | ACID AMIDE HYDROLASE | VAGAL AFFERENT NEURONS | CISPLATIN-INDUCED EMESIS | Cannabinoid Receptor Modulators - metabolism | Polyunsaturated Alkamides - chemistry | Gastrointestinal Diseases - physiopathology | Humans | Receptors, Cannabinoid - physiology | Arachidonic Acids - chemistry | Genetic Variation | Receptors, Cannabinoid - drug effects | Receptors, Cannabinoid - metabolism | Cannabinoid Receptor Modulators - physiology | Cannabis - chemistry | Gastrointestinal Tract - physiology | Gastrointestinal Diseases - drug therapy | Dronabinol - pharmacology | Drug Evaluation, Preclinical | Cannabinoids - metabolism | Endocannabinoids | Drug Tolerance | Gastrointestinal Tract - drug effects | Arachidonic Acids - pharmacology | Gastrointestinal Tract - metabolism | Cannabinoids - pharmacology | Cannabinoids - therapeutic use | Animals | Gastrointestinal Diseases - genetics | Models, Biological | Polyunsaturated Alkamides - pharmacology | Nitrogen oxide | Glycerol | Nerve growth factor | Lipase | Peptide hormones | Fatty acids | Glycerin | Cannabinoids | Gastrointestinal diseases | Physiological aspects | Phenols | Marijuana | Acetylcholine | Cholecystokinin | Vasoactive intestinal peptides | Health aspects | Mitogens
Journal Article
Journal Article
Journal of Clinical Gastroenterology, ISSN 0192-0790, 02/2016, Volume 50, Issue 2, pp. e13 - e18
Journal Article
Journal Article
Journal Article
British Journal of Nutrition, ISSN 0007-1145, 2014, Volume 112, Issue 4, pp. 536 - 546
In the present double-blind, randomised, parallel intervention study, the effects of the intake of galacto-oligosaccharides (GOS) on the gut microbiota of... 
Antibiotics | Galacto-oligosaccharides | Human intervention studies | Intestinal microbiota | BIFIDOBACTERIA | FECAL MICROBIOTA | FECES | DIETARY MODULATION | HUMAN INTESTINAL MICROBIOTA | IMPACT | NUTRITION & DIETETICS | PREBIOTICS | FERMENTATION | DIVERSITY | ANTIBIOTIC-TREATMENT | Lower Gastrointestinal Tract - drug effects | Follow-Up Studies | Humans | Diarrhea - prevention & control | Male | Enterobacteriaceae - isolation & purification | Prebiotics - adverse effects | Bifidobacterium - isolation & purification | Diarrhea - chemically induced | Bifidobacterium - growth & development | Intestinal Mucosa - drug effects | Young Adult | Feces - microbiology | Oligosaccharides - analysis | Bifidobacterium - metabolism | Adult | Female | Anti-Bacterial Agents - adverse effects | Lower Gastrointestinal Tract - microbiology | Enterobacteriaceae - growth & development | Double-Blind Method | Microbial Viability - drug effects | Oligosaccharides - therapeutic use | Oligosaccharides - adverse effects | Intestinal Mucosa - microbiology | Oligosaccharides - metabolism | Enterobacteriaceae - metabolism | Monosaccharides - analysis | Prebiotics - analysis | Bifidobacterium - drug effects | Feces - chemistry | Butyric Acid - metabolism | Adolescent | Butyric Acid - analysis | Enterobacteriaceae - drug effects | Amoxicillin - adverse effects | Monosaccharides - metabolism | Microbiology | Dietary supplements | dietary modulation | fecal microbiota | bifidobacteria | diversity | impact | prebiotics | fermentation | human intestinal microbiota | antibiotic-treatment | feces
Journal Article