Taladine Disease Interactions
There are 6 disease interactions with Taladine (ranitidine).
H2 antagonists (applies to Taladine) GI bleeding
Major Potential Hazard, Moderate plausibility. Applicable conditions: Gastrointestinal Hemorrhage
Histamine H2 receptor antagonists should not be used in the presence of vomit with blood, or bloody or black stools. These might be serious conditions and the diagnosis needs to be ruled out.
References
- "Product Information. Pepcid (famotidine)." Merck & Co., Inc PROD (2002):
- "Product Information. Axid (nizatidine)." Lilly, Eli and Company PROD (2002):
- "Product Information. Tagamet (cimetidine)." SmithKline Beecham PROD (2001):
- "Product Information. Tritec (ranitidine bismuth citrate)." Glaxo Wellcome PROD (2001):
- "Product Information. Zantac 75 (ranitidine)." Pfizer U.S. Pharmaceuticals (2002):
Ranitidine (applies to Taladine) porphyria
Major Potential Hazard, Moderate plausibility.
Ranitidine may rarely precipitate acute porphyria attacks and should be avoided in patients with a history of acute porphyria.
References
- "Product Information. Zantac (ranitidine)." Glaxo Wellcome PROD (2001):
Ranitidine (applies to Taladine) hemodialysis
Moderate Potential Hazard, High plausibility.
Ranitidine is partially removed by hemodialysis and should be administered after dialysis.
References
- Garg DC, Baltodano N, Perez GO, et al. "Pharmacokinetics of ranitidine after intravenous administration in hemodialysis patients." Pharmacology 31 (1985): 189-93
- Comstock TJ, Sica DA, Harford A, Eshelman F "Ranitidine bioavailability and disposition kinetics in patients undergoing chronic hemodialysis." Nephron 52 (1989): 15-9
- "Product Information. Zantac (ranitidine)." Glaxo Wellcome PROD (2001):
Ranitidine (applies to Taladine) liver disease
Moderate Potential Hazard, Low plausibility.
Ranitidine is partially metabolized by the liver. Although dosage reductions are generally not necessary, therapy with ranitidine should be administered cautiously in patients with liver disease. Elevated ALT (SGPT) has been observed in patients receiving ranitidine intravenously at dosages greater than those normally recommended for 5 days or more.
References
- Morichau-Beauchant M, Houin G, Mavier P, et al. "Pharmacokinetics and bioavailability of ranitidine in normal subjects and cirrhotic patients." Dig Dis Sci 31 (1986): 113-8
- Young CJ, Daneshmend TK, Roberts CJC "Effects of cirrhosis and ageing on the elimination and bioavailability of ranitidine." Gut 23 (1982): 819-23
- Gonzalez-Martin G, Paulos C, Veluso B, et al. "Ranitidine disposition in severe hepatic cirrhosis." Int J Clin Pharmacol Ther Toxicol 25 (1987): 139-42
- Smith IL, Ziemniak JA, Bernhard H, et al. "Ranitidine disposition and systemic availability in hepatic cirrhosis." Clin Pharmacol Ther 35 (1984): 487-94
- Okolicsanyi L, Venuti M, Strazzabosco M, et al. "Oral and intravenous pharmacokinetics of ranitidine in patients with liver cirrhosis." Int J Clin Pharmacol Ther Toxicol 22 (1984): 329-32
- "Product Information. Zantac (ranitidine)." Glaxo Wellcome PROD (2001):
Ranitidine (applies to Taladine) PKU
Moderate Potential Hazard, High plausibility. Applicable conditions: Phenylketonuria
Zantac (brand of ranitidine) 150 EFFERdose tablets and granules both contain 16.84 mg of phenylalanine per each 150 mg of ranitidine. The phenylalanine content should be considered when these products are used in patients who must restrict their intake of phenylalanine (i.e. phenylketonurics).
References
- "Product Information. Zantac (ranitidine)." Glaxo Wellcome PROD (2001):
Ranitidine (applies to Taladine) renal dysfunction
Moderate Potential Hazard, High plausibility.
Ranitidine is primarily eliminated by the kidney. Although the drug is generally well-tolerated, the daily dosage should initially be reduced in patients with moderate to severe renal impairment (CrCl < 50 mL/min). If necessary, the daily dosage may be increased with caution.
References
- McGonigle RJ, Williams LC, Amphlett GE, et al. "The pharmacokinetics of ranitidine in renal disease." Pharmacokinet Pharmacodynam (1982): 41-7
- Meffin PJ, Grgurinovich N, Brooks PM, et al. "Ranitidine disposition in patients with renal impairment." Br J Clin Pharmacol 16 (1983): 731-4
- Zech PY, Chau NP, Pozet N, et al. "Ranitidine kinetics in chronic renal impairment." Clin Pharmacol Ther 34 (1983): 667-72
- McFayden ML, Folb PI, Miller R, et al. "Pharmacokinetics of ranitidine in patients with chronic renal failure." Eur J Clin Pharmacol 25 (1983): 347-51
- Garg DC, Baltodano N, Jallad NS, et al. "Pharmacokinetics of ranitidine in patients with renal failure." J Clin Pharmacol 26 (1986): 286-91
- Kopitar Z, Cvelbar P, Zorz M, et al. "Pharmacokinetics of ranitidine in adult patients with end stage renal disease after single and multiple dosing." Acta Pharm Juglosl 37 (1987): 371-9
- "Product Information. Zantac (ranitidine)." Glaxo Wellcome PROD (2001):
- Dixon JS, Borgcostanzi JM, Langley SJ, Lacey LF, Toon S "The effect of renal function on the pharmacokinetics of ranitidine." Eur J Clin Pharmacol 46 (1994): 167-71
- Gladziwa U, Klotz U "Pharmacokinetic optimisation of the treatment of peptic ulcer in patients with renal failure." Clin Pharmacokinet 27 (1994): 393-408
Taladine drug interactions
There are 139 drug interactions with Taladine (ranitidine).
Taladine alcohol/food interactions
There is 1 alcohol/food interaction with Taladine (ranitidine).
More about Taladine (ranitidine)
- Check interactions
- Compare alternatives
- Latest FDA alerts (18)
- Side effects
- Dosage information
- During pregnancy
- Drug class: H2 antagonists
- Breastfeeding
Related treatment guides
Drug Interaction Classification
Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. | |
Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. | |
Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan. | |
No interaction information available. |
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.