Drug Interactions between hydroxychloroquine and Nolvadex
This report displays the potential drug interactions for the following 2 drugs:
- hydroxychloroquine
- Nolvadex (tamoxifen)
Interactions between your drugs
tamoxifen hydroxychloroquine
Applies to: Nolvadex (tamoxifen) and hydroxychloroquine
GENERALLY AVOID: Hydroxychloroquine (HCQ) and chloroquine (CQ) can cause dose-related retinal toxicity. The risk of retinal toxicity from HCQ or CQ increases with concurrent use of drugs known to induce retinal toxicity (e.g., tamoxifen), higher doses (greater than or equal to 5 mg/kg of actual body weight for HCQ and 2.3 mg/kg of actual body weight for chloroquine), treatment duration >5 years, low body weight, advanced age, and concomitant retinal, renal, or hepatic disease. The precise mechanism of retinal toxicity is unclear, but it is thought to be associated with high concentrations of 4-aminoquinoline (4-AQ) from HCQ and CQ in the ocular tissue, which binds to melanin in the retinal pigment epithelium (RPE), ultimately leading to inner and outer retinal damage. This damage disrupts crucial steps in the visual cycle, resulting in lipofuscin accumulation and photoreceptor degradation. Retinal toxicity is more commonly associated with CQ than with HCQ and can result in the development of circular defects (bull's eye maculopathy) and diametric defects of the retina. In a retrospective case-control study evaluating 2361 patients within an integrated health organization who had used HCQ continuously for at least 5 years, visual field (VF) testing or spectral-domain optical coherence tomography (SD-OCT) were used to identify the presence of retinal toxicity. The overall prevalence of retinopathy was 7.5% and increased significantly with higher daily doses (>5.0 mg/kg) and long-term use (>10 years). Additionally, concomitant use of tamoxifen with HCQ increased the risk of retinal toxicity by approximately 5-fold.
MANAGEMENT: Coadministration of hydroxychloroquine (HCQ) or chloroquine (CQ) with other drugs that can induce retinal toxicity (e.g., tamoxifen) should generally be avoided. If coadministration is required, ophthalmological examinations including best corrected distance visual acuity (BCVA), automated threshold VF and SD-OCT tests should be started one year after therapy is initiated and repeated annually. In addition, maintaining HCQ doses of <5 mg/kg of actual body weight and CQ doses of <2.3 mg/kg of actual body weight are recommended to reduce retinal toxicity risk. Individual product labeling and local guidelines should be consulted for additional guidance.
GENERALLY AVOID: Hydroxychloroquine (HCQ) and chloroquine (CQ) can cause dose-related prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the QT interval may result in additive effects and increased risk of ventricular arrhythmias including torsade de pointes and sudden death. In general, the risk of an individual agent or a combination of agents causing ventricular arrhythmia in association with QT prolongation is largely unpredictable but may be increased by certain underlying risk factors such advanced age, congenital long QT syndrome, cardiac disease, and electrolyte disturbances (e.g., hypokalemia, hypomagnesemia). In addition, the extent of drug-induced QT prolongation is dependent on the particular drug(s) involved and dosage(s) of the drug(s). In a retrospective study of electronic health records analyzing QTc prolongation risk in patients on HCQ alone or with other QT-prolonging drugs, a statistically significant QTc interval increase of 18 msec was observed in the HCQ monotherapy group. No significant QTc increase was found in patients taking HCQ with the evaluated QT-prolonging medications. However, this result may have been influenced by factors such as varying patient sensitivity to QT-prolonging drugs across treatment sites, and differences in HCQ exposure duration prior to QTc measurement in combination therapy cases.
MANAGEMENT: Coadministration of hydroxychloroquine (HCQ) or chloroquine (CQ) with other drugs that can prolong the QT interval should generally be avoided, particularly in patients with baseline QT prolongation (e.g., QTc greater than or equal to 500 msec) or congenital long QT syndrome. Close monitoring of QTc interval, electrolyte levels, and renal and hepatic function is recommended if concomitant use is required, and benefits are anticipated to outweigh the risks. Electrolyte abnormalities should be corrected prior to initiating treatment with hydroxychloroquine. Patients should be advised to seek prompt medical attention if they experience symptoms that could indicate the occurrence of torsade de pointes such as dizziness, lightheadedness, fainting, palpitation, irregular heart rhythm, shortness of breath, or syncope. Because hydroxychloroquine and chloroquine are eliminated slowly from the body (terminal half-lives: HCQ = 40-50 days, CQ = 10-60 days), potential drug interactions may persist for several weeks to months after their discontinuation.
References (13)
- (2024) "Product Information. Hydroxychloroquine Sulfate (hydroxychloroquine)." Dr. Reddy's Laboratories Inc
- (2023) "Product Information. Plaquenil (hydroxychloroquine)." Sanofi-Aventis Canada Inc
- (2024) "Product Information. Quinoric (hydroxychloroquine)." Bristol Laboratories Ltd
- (2024) "Product Information. Hydroxychloroquine (GH) (hydroxychloroquine)." Generic Health Pty Ltd
- (2023) "Product Information. HIDROXICLOROQUINA RATIOPHARM (hidroxicloroquina)." RATIOPHARM ESPANA S.A.
- Yusuf IH, Foot B, Ardern-Jones MR, et al. (2024) The Royal College of Ophthalmologists recommendations on screening for hydroxychloroquine and chloroquine users in the United Kingdom: executive summary https://pmc.ncbi.nlm.nih.gov/articles/PMC6043500/#:~:text=All%20individuals%20who%20have%20taken,rece
- Rosenbaum JT, Costenbader KH, Desmarais J (2024) American College of Rheumatology, American Academy of Dermatology, Rheumatologic Dermatology Society, and American Academy of Ophthalmology 2020 Joint Statement on Hydroxychloroquine Use With Respect to Retinal Toxicity https://acrjournals.onlinelibrary.
- melles rb, Marmor MF (2024) The risk of toxic retinopathy in patients on long-term hydroxychloroquine therapy https://pubmed.ncbi.nlm.nih.gov/25275721/
- carter kl, Do DV (2024) Hydroxychloroquine-induced Retinal Toxicity https://www.jrheum.org/content/47/4/632
- Schrezenmeier E, dorner t (2024) Mechanisms of action of hydroxychloroquine and chloroquine: implications for rheumatology https://sdpomf.com/ficheros/web/noticias/3b0aa45e04b3ae02ce7abc4db6abeff0e3b921878b0b38010d76a65548d652c6.pdf
- (2022) "Product Information. Avloclor (chloroquine)." Alliance Pharmaceuticals Ltd
- (2023) "Product Information. Chloroquine Phosphate (chloroquine)." Avet Pharmaceuticals Inc.
- (2022) "Product Information. RESOCHÍN (cloroquina)." KERN PHARMA, S.L.
Drug and food interactions
tamoxifen food
Applies to: Nolvadex (tamoxifen)
GENERALLY AVOID: Due to their estrogenic effect, isoflavones present in soy such as genistein and daidzein may stimulate breast tumor growth and antagonize the antiproliferative action of tamoxifen. Supportive data are derived primarily from in vitro and animal studies. In vitro, low concentrations of these phytoestrogens have been found to promote DNA synthesis and reverse the inhibitory effect of tamoxifen on estrogen-dependent breast cancer cell proliferation. In contrast, high concentrations of genistein greater than 10 microM/L have been found to enhance tamoxifen effects by inhibiting breast cancer cell growth. It is not known if these high concentrations are normally achieved in humans. Plasma concentrations below 4 microM/L have been observed in healthy volunteers given a soy diet for one month or large single doses of genistein. These concentrations are comparable to the low plasma concentrations associated with tumor stimulation reported in animals. In a study of 155 female breast cancer survivors with substantially bothersome hot flashes, a product containing 50 mg of soy isoflavones (40% to 45% genistein; 40% to 45% daidzein; 10% to 20% glycitein) taken three times a day was found to be no more effective than placebo in reducing hot flashes. No toxicity or recurrence of breast cancer was reported during the 9-week study period.
Green tea does not appear to have significant effects on the pharmacokinetics of tamoxifen or its primary active metabolite, endoxifen. In a study consisting of 14 patients who have been receiving tamoxifen treatment at a stable dose of 20 mg (n=13) or 40 mg (n=1) once daily for at least 3 months, coadministration with green tea supplements twice daily for 14 days resulted in no significant differences in the pharmacokinetics of either tamoxifen or endoxifen with respect to peak plasma concentration (Cmax), systemic exposure (AUC), and trough plasma concentration (Cmin) compared to administration of tamoxifen alone. The combination was well tolerated, with all reported adverse events categorized as mild (grade 1) and none categorized as serious or severe (grade 3 or higher) during the entire study. Although some adverse events such as headache, polyuria, gastrointestinal side effects (e.g., constipation, dyspepsia), and minor liver biochemical disturbances were reported more often during concomitant treatment with green tea, most can be attributed to the high dose of green tea used or to the caffeine in green tea. The green tea supplements used were 1000 mg in strength and contained 150 mg of epigallocatechin-3-gallate (EGCG), the most abundant and biologically active catechin in green tea. According to the investigators, the total daily dose of EGCG taken by study participants is equivalent to the amount contained in approximately 5 to 6 cups of regular green tea. However, it is not known to what extent the data from this study may be applicable to other preparations of green tea such as infusions, since the bioavailability of EGCG and other catechins may vary between preparations.
MANAGEMENT: Until more information is available, patients treated with tamoxifen may consider avoiding or limiting the consumption of soy-containing products. Consumption of green tea and green tea extracts during tamoxifen therapy appears to be safe.
References (2)
- Therapeutic Research Faculty (2008) Natural Medicines Comprehensive Database. http://www.naturaldatabase.com
- Braal CL, Hussaarts KGAM, Seuren L, et al. (2020) "Influence of green tea consumption on endoxifen steady-state concentration in breast cancer patients treated with tamoxifen." Breast Cancer Res Treat, 184, p. 107-13
hydroxychloroquine food
Applies to: hydroxychloroquine
GENERALLY AVOID: Theoretically, grapefruit and grapefruit juice may increase the plasma concentrations of hydroxychloroquine or chloroquine and the risk of toxicities such as QT interval prolongation and ventricular arrhythmias. The proposed mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall induced by certain compounds present in grapefruit. Following coadministration with cimetidine, a weak to moderate CYP450 3A4 inhibitor, a 2-fold increase in chloroquine exposure occurred. Since chloroquine and hydroxychloroquine have similar structures and metabolic elimination pathways, a similar interaction may be observed with hydroxychloroquine. In general, the effect of grapefruit juice is concentration-, dose- and preparation-dependent, and can vary widely among brands. Certain preparations of grapefruit juice (e.g., high dose, double strength) have sometimes demonstrated potent inhibition of CYP450 3A4, while other preparations (e.g., low dose, single strength) have typically demonstrated moderate inhibition. Pharmacokinetic interactions involving grapefruit juice are also subject to a high degree of interpatient variability, thus the extent to which a given patient may be affected is difficult to predict.
ADJUST DOSING INTERVAL: Administration with food or milk may reduce the incidence of hydroxychloroquine-related gastrointestinal adverse effects.
MANAGEMENT: Although clinical data are lacking, it may be advisable to avoid the consumption of grapefruit, grapefruit juice, and any supplement containing grapefruit extract during hydroxychloroquine or chloroquine therapy. Hydroxychloroquine should be administered with food or milk to reduce the occurrence of gastrointestinal upset.
References (5)
- (2024) "Product Information. Hydroxychloroquine Sulfate (hydroxychloroquine)." Dr. Reddy's Laboratories Inc
- (2023) "Product Information. Plaquenil (hydroxychloroquine)." Sanofi-Aventis Canada Inc
- (2024) "Product Information. Quinoric (hydroxychloroquine)." Bristol Laboratories Ltd
- (2024) "Product Information. Hydroxychloroquine (GH) (hydroxychloroquine)." Generic Health Pty Ltd
- (2023) "Product Information. HIDROXICLOROQUINA RATIOPHARM (hidroxicloroquina)." RATIOPHARM ESPANA S.A.
Therapeutic duplication warnings
No warnings were found for your selected drugs.
Therapeutic duplication warnings are only returned when drugs within the same group exceed the recommended therapeutic duplication maximum.
See also
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
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