7 Interactions found for:
Drug Interactions
Moderate
Metoprolol
+ Jardiance
The following applies to the ingredients: Metoprolol and Empagliflozin (found in Jardiance)
Professional Content
MONITOR: Sodium-glucose co-transporter 2 (SGLT-2) inhibitors may potentiate the hypotensive effects of antihypertensive agents, including beta-blockers. Inhibition of glucose and sodium co-transport produces mild diuresis and transient natriuresis, resulting in intravascular volume contraction. Volume depletion-related adverse reactions including hypotension, postural dizziness, orthostatic hypotension, syncope, and dehydration can occur after initiating treatment with SGLT-2 inhibitors, and the risk may be increased with concomitant use of other agents that can lower blood pressure.
MONITOR: Beta-blockers may inhibit some of the normal physiologic responses to hypoglycemia, which, when combined with antidiabetic agents such as sodium-glucose co-transporter 2 (SGLT-2) inhibitors, may potentiate the risk for adverse events. Symptoms of hypoglycemia, such as tremors and tachycardia, may be absent, making it more difficult for patients to recognize an oncoming episode. In addition, multiple effects on glucose metabolism have been reported, usually with the noncardioselective beta-blockers (e.g., propranolol, pindolol, timolol) but occasionally also with relatively beta-1 selective agents (e.g., atenolol, metoprolol, nebivolol). Specifically, inhibition of catecholamine-mediated glycogenolysis and glucose mobilization in association with beta-blockade can potentiate insulin-induced hypoglycemia in diabetics and delay the recovery of normal blood glucose levels. Prolonged and severe hypoglycemia may occur, although these events have rarely been reported. Significant increases in blood pressure and bradycardia can also occur during hypoglycemia in diabetics treated with insulin and beta-blockers due to the antagonism of epinephrine's effect on beta-2 adrenergic receptors, which leads to unopposed alpha-adrenergic effects, including vasoconstriction. On the other hand, decreased glucose tolerance and decreased glucose-induced insulin secretion have also been reported with various beta-blockers. For example, cardioselective beta-blockers like atenolol have been noted to increase insulin resistance while others such as metoprolol and the noncardioselective propranolol are known to increase hepatic glycogenolysis and gluconeogenesis, which may contribute to hyperglycemia. However, beta-blockers with intrinsic sympathomimetic activity and alpha-adrenergic activity, such as pindolol, or those with alpha-blocking effects, such as carvedilol, are reported to have a lesser impact on insulin sensitivity and may even have neutral or mildly positive effects on glycemic control due to vasodilating and insulin-sensitizing effects. The extent to which these opposing effects manifest clinically and whether one effect will predominate are unclear.
MANAGEMENT: Caution is advised if SGLT-2 inhibitors are coadministered with beta-blockers, particularly in the elderly and patients with impaired renal function. Prior to initiating SGLT-2 inhibitors, volume status should be assessed and corrected, if necessary. If volume depletion occurs, treatment with SGLT-2 inhibitors should be interrupted until the condition is corrected. Clinical and laboratory monitoring are recommended during therapy, including electrolytes, fluid status, renal function, and blood pressure. In addition, cardioselective beta-blockers are generally considered safer than noncardioselective agents in the treatment of diabetic patients. Nevertheless, caution is advised if they are prescribed to patients on SGLT-2 inhibitor therapy, as cardioselectivity is not absolute and larger doses of beta-1 selective agents may pose some of the same risks as nonselective agents. Patients should be advised of the need for regular blood glucose monitoring, due to the potential for developing hypoglycemia or hyperglycemia. They should also be made aware that certain symptoms of hypoglycemia such as tremor and tachycardia may be masked. However, other symptoms such as headache, dizziness, drowsiness, confusion, nausea, hunger, weakness, and perspiration may be unaffected. The same precautions are applicable in diabetic patients treated with ophthalmic beta-blockers.
References
- Shepherd AM, Lin M-S, Keeton TK "Hypoglycemia-induced hypertension in a diabetic patient on metoprolol." Ann Intern Med 94 (1981): 357-8
- Micossi P, Pollavini G, Raggi U, et al. "Effects of metoprolol and propranolol on glucose tolerance and insulin secretion in diabetes mellitus." Horm Metab Res 16 (1984): 59-63
- Popp DA, Tse TF, Shah SD, et al. "Oral propranolol and metoprolol both impair glucose recovery from insulin-induced hypoglycemia in insulin-dependent diabetes mellitus." Diabetes Care 7 (1984): 243-7
- Mann SJ, Krakoff LR "Hypertensive crisis caused by hypoglycemia and propranolol." Arch Intern Med 144 (1984): 2427-8
- Groop L, Totterman KJ, Harno K, Gordin A "Influence of beta-blocking drugs on glucose metabolism in patients with non-insulin dependent diabetes mellitus." Acta Med Scand 211 (1982): 7-12
- Viberti GC, Keen H, Bloom SR "Beta blockade and diabetes mellitus: effect of oxprenolol and metoprolol on the metabolic, cardiovascular, and hormonal response to insulin-induced hypoglycemia in insulin-dependent diabetics." Metabolism 29 (1980): 873-9
- Viberti GC, Keen H, Bloom SR "Beta blockade and diabetes mellitus: effect of oxprenolol and metoprolol on the metabolic, cardiovascular, and hormonal response to insulin-induced hypoglycemia in normal subjects." Metabolism 29 (1980): 866-72
- Newman RJ "Comparison of propranolol, metoprolol, and acebutolol on insulin-induced hypoglycaemia." Br Med J 2 (1976): 447-9
- Smith U "Beta blockade in diabetes." N Engl J Med 299 (1978): 1467
- Zaman R, Kendall MJ, Biggs PI "The effect of acebutolol and propranolol on the hypoglycaemic action of glibenclamide." Br J Clin Pharmacol 13 (1982): 507-12
- Munroe WP, Rindone JP, Kershner RM "Systemic side effects associated with the ophthalmic administratiion of timolol." Drug Intell Clin Pharm 19 (1985): 85-9
- Ostman J "B-adrenergic blockade and diabetes mellitus." Acta Med Scand 672 (1983): 69-77
- Deacon SP, Karunanayake A, Barnett D "Acebutolol, atenolol, and propranolol and metabolic responses to acute hypoglycaemia in diabetes." Br Med J 12 (1977): 1255-7
- Pollare T, Lithell H, Selinus I, Berne C "Sensitivity to insulin during treatment with atenolol and metoprolol: a randomised, double blind study of effects on carbohydrate and lipoprotein metabolism in hypertensive patients." BMJ 298 (1989): 1152-7
- Sinclair AJ, Davies IB, Warrington SJ "Betaxolol and glucose-insulin relationships: studies in normal subjects taking glibenclamide or metformin." Br J Clin Pharmacol 30 (1990): 699-702
- "New Zealand Committee on Adverse Drug Reactions. Ninth Annual Report." N Z Dent J 71 (1975): 28-32
- "Product Information. Invokana (canagliflozin)." Janssen Pharmaceuticals (2013):
- "Product Information. Farxiga (dapagliflozin)." Bristol-Myers Squibb (2014):
- "Product Information. Jardiance (empagliflozin)." Boehringer Ingelheim (2014):
- "Product Information. Brenzavvy (bexagliflozin)." TheracosBio, LLC (2023):
- "Product Information. Sidapvia 10/100 (dapagliflozin-siTagliptin)." AstraZeneca Pty Ltd VV-RIM-06210739 v 1. (2024):
- Wilcox CS "Antihypertensive and Renal Mechanisms of SGLT2 (Sodium-Glucose Linked Transporter 2) Inhibitors" AHA/ASA Journal 75 (2020): 894 - 901
- hasan a, menon n, Zerin F "Dapagliflozin induces vasodilation in resistance-size mesenteric arteries by stimulating smooth muscle cell KV7 ion channels" Heliyon 8 (2022): e09503
- Husam G, Manav B, green k "Dapagliflozin reduces systolic blood pressure and modulates vasoactive factors" DOM Journal 7 (2021): 1614-1623
- Sirenko Y, Rekovets O, Torbas O, et al. "Effect of Beta - Blockers on Insulin Resistance in Patients with Hypertension and Metabolic Syndrome after 6 Months of Treatment" J Endocrinol Diab 4 (2017): 1-11
Drug and Food Interactions
Moderate
Metoprolol
+ Food
The following applies to the ingredients: Metoprolol
Food can enhance the levels of metoprolol in your body. You should take metoprolol at the same time each day, preferably with or immediately following meals. This will make it easier for your body to absorb the medication. Avoid drinking alcohol, which could increase drowsiness and dizziness while you are taking metoprolol. Metoprolol is only part of a complete program of treatment that also includes diet, exercise, and weight control. Follow your diet, medication, and exercise routines very closely.
The following applies to the ingredients: Metoprolol
Using metoprolol together with multivitamin with minerals may decrease the effects of metoprolol. Separate the administration times of metoprolol and multivitamin with minerals by at least 2 hours. If your doctor does prescribe these medications together, you may need a dose adjustment or special test to safely use both medications. It is important to tell your doctor about all other medications you use, including vitamins and herbs. Do not stop using any medications without first talking to your doctor.
Moderate
Jardiance
+ Food
The following applies to the ingredients: Empagliflozin (found in Jardiance)
Alcohol may affect blood glucose levels in patients with diabetes. Both hypoglycemia (low blood sugar) and hyperglycemia (high blood sugar) may occur, depending on how much and how often you drink. You should avoid using alcohol if your diabetes is not well controlled or if you have high triglycerides, neuropathy (nerve damage), or pancreatitis. Moderate alcohol consumption generally does not affect blood glucose levels if your diabetes is under control. However, it may be best to limit alcohol intake to one drink daily for women and two drinks daily for men (1 drink = 5 oz wine, 12 oz beer, or 1.5 oz distilled spirits) in conjunction with your normal meal plan. Avoid drinking alcohol on an empty stomach or following exercise, as it may increase the risk of hypoglycemia. It is important to tell your doctor about all other medications you use, including vitamins and herbs. Do not stop using any medications without first talking to your doctor.
Drug and Pregnancy Interactions
Major
Metoprolol
+ Pregnancy
The following applies to the ingredients: Metoprolol
Professional Content
Safety has not been established during pregnancy.
-According to some authorities: Use is not recommended unless benefit outweighs risk; if used during pregnancy, administer the lowest possible dose and discontinue at least 2 to 3 days prior to expected delivery, if possible.
AU TGA pregnancy category: C
US FDA pregnancy category: Not assigned
Risk summary: Inconclusive data available on the use of this drug in pregnant women to inform a drug-related risk.
Comments:
-Based on published literature, this drug may cause erectile dysfunction and inhibit sperm motility.
Animal studies have revealed increased post-implantation loss, fetolethality, and decreased neonatal survival. This drug crosses placenta, neonates born to mothers who are receiving metoprolol during pregnancy, may be at risk for hypotension, hypoglycemia, bradycardia, and respiratory depression.
AU TGA pregnancy category C: Drugs which, owing to their pharmacological effects, have caused or may be suspected of causing, harmful effects on the human fetus or neonate without causing malformations. These effects may be reversible. Accompanying texts should be consulted for further details.
US FDA pregnancy category Not Assigned: The US FDA has amended the pregnancy labeling rule for prescription drug products to require labeling that includes a summary of risk, a discussion of the data supporting that summary, and relevant information to help health care providers make prescribing decisions and counsel women about the use of drugs during pregnancy. Pregnancy categories A, B, C, D, and X are being phased out.
References
- "Product Information. Lopressor (metoprolol)." Novartis Pharmaceuticals PROD (2001):
- Cerner Multum, Inc. "UK Summary of Product Characteristics." O 0
- Cerner Multum, Inc. "Australian Product Information." O 0
- "Product Information. Kapspargo Sprinkle (metoprolol)." Sun Pharmaceutical Industries (2023):
- "Product Information. Toprol-XL (metoprolol)." Melinta Therapeutics, Inc. (2023):
- "Product Information. Lopressor (metoprolol)." Validus Pharmaceuticals LLC (2025):
- "Product Information. Metoprolol Tartrate (metoprolol)." Hikma USA (formerly West-Ward Pharmaceutical Corporation) (2025):
Major
Jardiance
+ Pregnancy
The following applies to the ingredients: Empagliflozin (found in Jardiance)
Professional Content
Use should be avoided, especially during the second and third trimesters of pregnancy.
AU TGA pregnancy category: D
US FDA pregnancy category: Not Assigned
Risk Summary: There is limited data in pregnant women to determine a drug-associated risk for major birth defects and miscarriage. Based on animal data, this drug may cause adverse renal effects in the developing fetus.
Comments:
-Poorly controlled diabetes in pregnancy increases the risk of adverse maternal and fetal outcomes.
Animal studies have revealed evidence of adverse renal changes and embryofetal toxicity. Administration of this drug to pregnant animals during the period of organogenesis at doses up to 154 times the maximum clinical dose based on AUC resulted in maternal/fetal toxicity, malformations, and reduced offspring body weights. In juvenile rats, direct exposure to this drug at doses approximately 13 times the maximum clinical dose caused increased kidney weights and renal tubular/pelvic dilatations. These findings occurred during a period of renal development in rats corresponding to the late second and third trimester of human renal development. Animal studies do not indicate direct or indirect harmful effects with respect to fertility. There are no controlled data in human pregnancy.
Poorly controlled diabetes in pregnancy increases the maternal risk for diabetic ketoacidosis, pre-eclampsia, spontaneous abortions, preterm delivery, stillbirth, and delivery complications. Fetal risks of poorly controlled diabetes in pregnancy include an increased risk for major birth defects, stillbirth, and macrosomia-related morbidity.
AU TGA pregnancy category D: Drugs which have caused, are suspected to have caused or may be expected to cause, an increased incidence of human fetal malformations or irreversible damage. These drugs may also have adverse pharmacological effects. Accompanying texts should be consulted for further details.
US FDA pregnancy category Not Assigned: The US FDA has amended the pregnancy labeling rule for prescription drug products to require labeling that includes a summary of risk, a discussion of the data supporting that summary, and relevant information to help health care providers make prescribing decisions and counsel women about the use of drugs during pregnancy. Pregnancy categories A, B, C, D, and X are being phased out.
References
- "Product Information. Jardiance (empagliflozin)." Boehringer Ingelheim Ltd (2023):
- "Product Information. Jardiance (empagliflozin)." Boehringer Ingelheim SUPPL-42 (2023):
- "Product Information. Jardiance (empagliflozin)." Boehringer Ingelheim Pty Ltd (2024):
Drug and Breastfeeding Interactions
Major
Metoprolol
+ Breastfeeding
The following applies to the ingredients: Metoprolol
Professional Content
AU and UK: Use is not recommended unless benefit outweighs risk.
US: This drug has been used without apparent harmful effects; caution is recommended.
Excreted into human milk: Yes (in small amounts)
Comments: This drug has been used without apparent harmful effects in the nursing infant.
An infant consuming 1 L of breast milk a day would receive a dose of less than 1 mg of drug.
References
- "Product Information. Lopressor (metoprolol)." Novartis Pharmaceuticals PROD (2001):
- Cerner Multum, Inc. "UK Summary of Product Characteristics." O 0
- Cerner Multum, Inc. "Australian Product Information." O 0
Major
Jardiance
+ Breastfeeding
The following applies to the ingredients: Empagliflozin (found in Jardiance)
Professional Content
Use is not recommended
Excreted into human milk: Unknown
Excreted into animal milk: Yes
Comments:
-A risk to the breastfed infant cannot be excluded; there is a potential for serious adverse effects on postnatal renal development.
-An alternate drug may be preferred, especially while nursing a newborn or preterm infant.
Drug accumulation was observed in the milk of lactating animals. Studies in juvenile rats with direct exposure demonstrated pelvic and tubular dilations of the kidney during maturation. Human kidney maturation occurs in utero and during the first 2 years of life; thus, a potential for serious harm to the developing kidney may exist for infants exposed to this drug during breastfeeding. However, some experts anticipate low amounts of this drug in human breastmilk due to high levels of plasma protein binding.
References
- "Product Information. Jardiance (empagliflozin)." Boehringer Ingelheim Ltd (2023):
- "Product Information. Jardiance (empagliflozin)." Boehringer Ingelheim SUPPL-42 (2023):
- Bethesda (MD): National Institute of Child Health and Human Development (US) "Empagliflozin - Drugs and Lactation Database (LactMed) https://www.ncbi.nlm.nih.gov/books/NBK500972/" (2023):
- "Product Information. Jardiance (empagliflozin)." Boehringer Ingelheim Pty Ltd (2024):
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.
Switch to: Professional Interactions
Drug Interaction Classification | |
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These classifications are only a guideline. The relevance of a particular drug interaction to a specific individual is difficult to determine. Always consult your healthcare provider before starting or stopping any medication. |
|
Major | Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. |
Moderate | Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. |
Minor | 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. |
Unknown | No interaction information available. |
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