Acyclovir (Injection) interactions
Full monograph for Acyclovir (Injection)Check it against another medicine
Medicines
563 documented
| Medicine | Severity | Mechanism | Effect | Sources |
|---|---|---|---|---|
| Everolimus | Major | Synergy | Coadministration of macrolide immunosuppressants with other nephrotoxic agents may increase the risk and/or severity of renal impairment due to additive… | 4 sources — open the full entry |
| Iodixanol | Major | Synergy | Concomitant use of intravascular radiocontrast media with other nephrotoxic agents may potentiate the risk of contrast-induced nephropathy and renal… | 7 sources — open the full entry |
| Iohexol | Major | Synergy | Concomitant use of intravascular radiocontrast media with other nephrotoxic agents may potentiate the risk of contrast-induced nephropathy and renal… | 7 sources — open the full entry |
| Iopamidol | Major | Synergy | Concomitant use of intravascular radiocontrast media with other nephrotoxic agents may potentiate the risk of contrast-induced nephropathy and renal… | 7 sources — open the full entry |
| Tacrolimus MonohydrateOralTopical | Major | Synergy | Coadministration of macrolide immunosuppressants with other nephrotoxic agents may increase the risk and/or severity of renal impairment due to additive… | 4 sources — open the full entry |
| Tenofovir Alafenamide | Major | Excretion | Coadministration of tenofovir with other nephrotoxic agents may increase the risk of renal impairment due to additive effects on the kidney. Additionally… | 8 sources — open the full entry |
| Tenofovir Disoproxil | Major | Excretion | Coadministration of tenofovir with other nephrotoxic agents may increase the risk of renal impairment due to additive effects on the kidney. Additionally… | 8 sources — open the full entry |
| Tizanidine Hydrochloride | Major | Metabolism | Coadministration with inhibitors of CYP450 1A2 may significantly increase the plasma concentrations and pharmacologic effects of tizanidine, which is a… | 8 sources — open the full entry |
| Bacitracin Zinc + Polymyxin B Sulfate | Moderate | Synergy · Unknown | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity.2 documented mechanisms | 2 sources — open the full entry |
| Ceftazidime + Avibactam | Moderate | Synergy | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity. Patients who are elderly… | 2 sources — open the full entry |
| Ceftazidime Pentahydrate | Moderate | Synergy | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity. Patients who are elderly… | 2 sources — open the full entry |
| Colistimethate Sodium | Moderate | Synergy | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity. | 2 sources — open the full entry |
| Cyclosporine (Oral) | Moderate | Synergy | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity. Patients who are elderly… | 2 sources — open the full entry |
| Dexamethasone + Neomycin Sulphate + Polymyxin B Sulphate | Moderate | Synergy · Unknown | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity.3 documented mechanisms | 2 sources — open the full entry |
| Entecavir Monohydrate | Moderate | Excretion | Coadministration of entecavir with another drug that is also eliminated by active tubular secretion may result in increased plasma concentrations of one or… | 2 sources — open the full entry |
| Fosphenytoin Sodium | Moderate | Others | A case report suggests that plasma phenytoin concentrations may be decreased in the presence of acyclovir. Seizure activity may increase. The mechanism is… | 17 sources — open the full entry |
| Gramacidin + Neomycin + Polymixin B | Moderate | Synergy · Unknown | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity.2 documented mechanisms | 2 sources — open the full entry |
| Hydrocortisone + Neomycin Sulphate + Polymixin B | Moderate | Synergy · Unknown | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity.3 documented mechanisms | 2 sources — open the full entry |
| Ifosfamide | Moderate | Synergy | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity. Patients who are elderly… | 2 sources — open the full entry |
| Lithium Carbonate | Moderate | Excretion | Acyclovir may significantly increase the serum levels of lithium. Acyclovir may competitively inhibit the glomerular filtration of lithium, and this… | 5 sources — open the full entry |
| Mesalazine [5-aminosalicylic acid] | Moderate | Synergy | Coadministration of 5-aminosalicylate with other nephrotoxic agents may increase the risk and severity of renal impairment due to additive effects on the… | 4 sources — open the full entry |
| Metronidazole + Neomycin Sulphate + Polymyxin B + Nystatin | Moderate | Synergy · Unknown | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity.4 documented mechanisms | 2 sources — open the full entry |
| Neomycin Sulfate + Bacitracin Zinc + Polymyxin B Sulfate | Moderate | Synergy · Unknown | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity.3 documented mechanisms | 2 sources — open the full entry |
| Neomycin Sulphate + Polymyxin B Sulphate + Pramoxine | Moderate | Synergy · Unknown | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity.2 documented mechanisms | 2 sources — open the full entry |
| Oxytetracycline + Polymixin B Sulphate | Moderate | Synergy | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity. | 2 sources — open the full entry |
| Pemetrexed | Moderate | Excretion | Coadministration with drugs that are eliminated by active tubular secretion may delay and/or decrease the clearance of pemetrexed. The mechanism is competitive… | 1 sources — open the full entry |
| Pethidine Hydrochloride | Moderate | Others | Acyclovir may increase the plasma concentrations of meperidine and normeperidine, the metabolite that has been associated with adverse effects such as… | 2 sources — open the full entry |
| Phenytoin Sodium | Moderate | Others | A case report suggests that plasma phenytoin concentrations may be decreased in the presence of acyclovir. Seizure activity may increase. The mechanism is… | 17 sources — open the full entry |
| Polymyxin B Sulfate | Moderate | Synergy | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity. | 2 sources — open the full entry |
| Prednisolone + Neomycin Sulphate + Polymixin B Sulphate | Moderate | Synergy · Unknown | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity.3 documented mechanisms | 2 sources — open the full entry |
| Ramelteon | Moderate | Metabolism | Coadministration with inhibitors of CYP450 1A2 may increase the plasma concentrations and pharmacologic effects of ramelteon, which is primarily metabolized by… | 2 sources — open the full entry |
| Remdesivir | Moderate | Excretion | Coadministration of remdesivir with nephrotoxic agents may increase the plasma concentrations of its main metabolite, GS-441524, and the excipient… | 5 sources — open the full entry |
| Sulfasalazine | Moderate | Synergy | Coadministration of 5-aminosalicylate with other nephrotoxic agents may increase the risk and severity of renal impairment due to additive effects on the… | 4 sources — open the full entry |
| Trospium Chloride | Moderate | Excretion | Theoretically, coadministration of trospium chloride with other drugs that are eliminated by active tubular secretion may result in increased plasma… | 4 sources — open the full entry |
| Aminophylline | Minor | Metabolism | Limited data suggest that the combination of a methyl xanthine with acyclovir may lead to elevated theophylline levels potentiating pharmacologic and adverse… | 4 sources — open the full entry |
| Lamivudine + Zidovudine | Minor | Others · Unknown | Excessive lethargy has been reported in some patients with coadministration of acyclovir and zidovudine. Concomitant use of these drugs in large trials has not…2 documented mechanisms | 11 sources — open the full entry |
| Lamivudine + Zidovudine + Nevirapine | Minor | Others · Unknown | Excessive lethargy has been reported in some patients with coadministration of acyclovir and zidovudine. Concomitant use of these drugs in large trials has not…3 documented mechanisms | 11 sources — open the full entry |
| Memantine + Donepezil | Minor | Excretion · Unknown | Theoretically, the concomitant administration of memantine and other drugs that undergo active renal tubular secretion may result in altered plasma levels of…2 documented mechanisms | 5 sources — open the full entry |
| Memantine Hydrochloride | Minor | Excretion | Theoretically, the concomitant administration of memantine and other drugs that undergo active renal tubular secretion may result in altered plasma levels of… | 5 sources — open the full entry |
| Mycophenolate Mofetil | Minor | Excretion | Coadministration with mycophenolic acid may increase the plasma concentrations of acyclovir. The mechanism of interaction has not been described. However… | 4 sources — open the full entry |
| Mycophenolic acid | Minor | Excretion | Coadministration with mycophenolic acid may increase the plasma concentrations of acyclovir. The mechanism of interaction has not been described. However… | 4 sources — open the full entry |
| Theophylline | Minor | Metabolism | Limited data suggest that the combination of a methyl xanthine with acyclovir may lead to elevated theophylline levels potentiating pharmacologic and adverse… | 4 sources — open the full entry |
Conditions
Conditions in which Acyclovir (Injection) needs care, as documented in this source.
Kidney Diseases
MajorAcyclovir is primarily eliminated by the kidney. Patients with renal impairment may be at greater risk for neuro- and nephrotoxicity (including further deterioration in renal function, tubular damage and acute renal failure) from acyclovir due to decreased drug clearance. Therapy with acyclovir should be administered cautiously in patients with renal impairment. Dosage adjustments are recommended in patients with moderate to severe renal dysfunction.
13 sources
- Laskin OL, Longstreth JA, Whelton A, et al. "Effect of renal failure on the pharmacokinetics of acyclovir." Am J Med 73 (1982): 197-201
- Laskin OL, Longstreth JA, Whelton A, et al. "Acyclovir kinetics in end-stage renal disease." Clin Pharmacol Ther 31 (1982): 594-600
- Sawyer MH, Webb DE, Balow JE, Straus SE "Acyclovir-induced renal failure." Am J Med 84 (1988): 1067-71
- Fletcher CV, Chinnock BJ, Chace B, Balfour HH "Pharmacokinetics and safety of high-dose oral acyclovir for suppression of cytomegalovirus disease after renal transplantation." Clin Pharmacol Ther 44 (1988): 158-63
- Rashed A, Asadeh B, Romeh SHA "Acyclovir-induced acute tubulo-interstitial nephritis." Nephron 56 (1990): 436-8
- Peterslund NA, Larsen ML, Mygind H "Acyclovir crystalluria." Scand J Infect Dis 20 (1988): 225-8
- Gnann JW, Barton NH, Whitley RJ "Acyclovir: mechanism of action, pharmacokinetics, safety and clinical applications." Pharmacotherapy 3 (1983): 275-83
- Hernandez E, Praga M, Moreno F, Montoyo C "Acute renal failure induced by oral acyclovir." Clin Nephrol 36 (1991): 155-6
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- Bianchetti MG, Roduit C, Oetliker OH "Acyclovir-induced renal failure: course and risk factors." Pediatr Nephrol 5 (1991): 238-9
- "Product Information. Zovirax (acyclovir)." Mylan Pharmaceuticals Inc (2017):
- Becker BN, Fall P, Hall C, Milam D, Leonard J, Glick A, Schulman G "Rapidly progressive acute renal failure due to acyclovir: case report and review of the literature." Am J Kidney Dis 22 (1993): 611-5
- Krieble BF, Rudy DW, Glick MR, Clayman MD "Case report: acyclovir neurotoxicity and nephrotoxicity--the role for hemodialysis." Am J Med Sci 305 (1993): 36-9
- Johnson GL, Limon L, Trikha G, Wall H "Acute renal failure and neurotoxicity following oral acyclovir." Ann Pharmacother 28 (1994): 460-3
Dehydration
ModerateAcyclovir crystals may precipitate in the renal tubules, particularly when the drug is injected intravenously as a bolus. Abnormal renal function may occur, which is usually reversible but may infrequently progress to tubular damage and acute renal failure. Patients who are dehydrated may be at increased risk for nephrotoxicity from acyclovir administration. Intravenous acyclovir should be administered over a one-hour period accompanied by adequate hydration. The urine flow should be monitored, especially within the first two hours following infusion when maximum urine concentration occurs. The recommended urine output is a minimum of 500 mL per gram of drug infused.
1 source
- "Product Information. Zovirax (acyclovir)." Mylan Pharmaceuticals Inc (2017):
Diseases requiring hemodialysis
ModerateAcyclovir is substantially removed by hemodialysis. Plasma levels of acyclovir have been shown to reduce by 60% following 6 hours of dialysis. Acyclovir should be administered after hemodialysis. Otherwise, an additional dose may be given after each hemodialysis session.
2 sources
- Krasny HC, Liao SH, de Miranda P, Laskin OL, Whelton A, Lietman PS "Influence of hemodialysis on acyclovir pharmacokinetics in patients with chronic renal failure." Am J Med 73 (1982): 202-4
- "Product Information. Zovirax (acyclovir)." Mylan Pharmaceuticals Inc (2017):
Neurotoxicity Syndromes
ModerateAcyclovir, particularly when administered intravenously in higher dosages, may occasionally produce neurotoxicity characterized by lethargy, obtundation, tremors, confusion, hallucinations, agitation, seizures, or coma. Therapy with acyclovir should be administered cautiously in the elderly and in patients with underlying neurologic abnormalities, severe renal or liver disease, or significant electrolyte abnormalities or hypoxia.
12 sources
- Jones PG, Beier-Hanratty SA "Acyclovir: neurologic and renal toxicity." Ann Intern Med 104 (1986): 892
- Fletcher CV, Chinnock BJ, Chace B, Balfour HH "Pharmacokinetics and safety of high-dose oral acyclovir for suppression of cytomegalovirus disease after renal transplantation." Clin Pharmacol Ther 44 (1988): 158-63
- Feldman S, Rodman J, Gregory B "Excessive serum concentrations of acyclovir and neurotoxicity." J Infect Dis 157 (1988): 385-8
- Cohen SM, Minkove JA, Zebley JW, Mulholland JH "Severe but reversible neurotoxicity from acyclovir." Ann Intern Med 100 (1984): 920
- Wade JC, Meyers JD "Neurologic symptoms associated with parenteral acyclovir treatment after marrow transplantation." Ann Intern Med 98 (1983): 921-5
- Bean B, Aeppli D "Adverse effects of high-dose intravenous acyclovir in ambulatory patients with acute herpes zoster." J Infect Dis 151 (1985): 362-5
- Gill MJ, Burgess E "Neurotoxicity of acyclovir in end stage renal disease." J Antimicrob Chemother 25 (1990): 300-1
- MacDiarmaid-Gordon AR, O'Connor M, Beaman M, Ackrill P "Neurotoxicity associated with oral acyclovir in patients undergoing dialysis." Nephron 62 (1992): 280-3
Show all 12 sourcesShow fewer sources
- "Product Information. Zovirax (acyclovir)." Mylan Pharmaceuticals Inc (2017):
- Krieble BF, Rudy DW, Glick MR, Clayman MD "Case report: acyclovir neurotoxicity and nephrotoxicity--the role for hemodialysis." Am J Med Sci 305 (1993): 36-9
- Rashiq S, Briewa L, Mooney M, Giancarlo T, Khatib R, Wilson FM "Distinguishing acyclovir neurotoxicity from encephalomyelitis." J Intern Med 234 (1993): 507-11
- Johnson GL, Limon L, Trikha G, Wall H "Acute renal failure and neurotoxicity following oral acyclovir." Ann Pharmacother 28 (1994): 460-3