JARDIANCE® (Empagliflozin)

The content on this website is in relation to adult patients

 

Safety Profile

Adverse reactions from reported placebo-controlled studies and post-marketing experience with JARDIANCE® (empagliflozin)1

Please consult the SmPC for further details regarding adverse events, monitoring requirements, contraindications and interactions prior to initiating JARDIANCE.

System organ classVery common (≥1/10)Common
(≥1/100 to <1/10)
Uncommon
(≥1/1,000 to <1/100)
Rare
(≥1/10,000 to <1/1,000)
Very rare (<1/10,000)
Infections and infestations 

Vaginal moniliasis, vulvovaginitis, balanitis and other genital infection

*Urinary tract infection (including pyelonephritis and urosepsis)*

 

 Necrotising fasciitis of the perineum (Fournier’s gangrene)** 
Metabolism and nutrition disordersHypoglycaemia
(when used with sulphonylurea or insulin)*
ThirstKetoacidosis**  
Gastrointestinal disorders Constipation   
Skin and subcutaneous tissue disorders Pruritus (generalised) RashUrticaria Angioedema  
Vascular disordersVolume depletion*    
Renal and urinary disorders Increased urination*Dysuria Tubulointerstitial nephritis
Investigations Serum lipids increased*

Blood creatinine increased/ Glomerular filtration rate decreased*

Haematocrit increased*
  

*See in section 4.8 of the SmPC for additional information.

**See below and section 4.4 of SmpC for further details.

Further safety information across all indications

Empagliflozin is not recommended in severe hepatic impairment, breastfeeding, type 1 diabetes, and is contraindicated in patients with hypersensitivity to the active ingredient or any of its excipients. Empagliflozin should be avoided in pregnancy.

Ketoacidosis

  • Rare cases of ketoacidosis, including life-threatening and fatal cases, have been reported in patients with diabetes mellitus treated with SGLT2 inhibitors, including JARDIANCE1
  • Symptomatic or unwell patients should be assessed for ketoacidosis immediately, regardless of blood glucose level. JARDIANCE should be discontinued immediately if ketoacidosis is suspected or diagnosed. Restarting SGLT2 inhibitor treatment after ketoacidosis is not recommended unless another clear precipitating factor is identified and resolved1
  • Suspend JARDIANCE for major surgical procedures or acute serious medical illnesses; Restart when ketone values are normal and the patient’s condition has stabilised1
  • SGLT2 inhibitors should be used with caution in patients who may have a higher risk of ketoacidosis, e.g. those with a low beta-cell function reserve, those with restricted food intake, severe dehydration or reduced insulin doses, or those with increased insulin doses due acute medical illness, surgery or alcohol abuse1
  • Refer to Section 4.4 of the SmPC for more details

Hypoglycaemia

  • No increase in major hypoglycaemia was observed with empagliflozin compared to placebo as monotherapy or add-on to metformin1
  • JARDIANCE® (empagliflozin) has an increased risk of hypoglycaemia when added to SU or insulin and is cited as very common adverse event in SmPC1
  • Consider lowering the dose of SU or insulin to reduce the risk of hypoglycaemia1

Genital infections & UTIs

  • Genital infections (e.g. thrush) were mild or moderate in intensity1 and rarely led to discontinuation of JARDIANCE2
  • Temporary interruption of JARDIANCE should be considered in patients with complicated UTIs1

Dehydration

  • JARDIANCE® (empagliflozin) may add to the diuretic effect of thiazide and loop diuretics and may increase the risk of dehydration and hypotension1
  • Monitor your patients' volume status and adjust diuretics as appropriate. Consider temporary interruption of JARDIANCE until fluid loss is corrected1

Necrotising fasciitis of the perineum (Fournier's gangrene)

  • Fournier’s gangrene has been reported in T2D patients taking SGLT2 inhibitors as a rare (≥1/10 000 to <1/1 000) but serious event that requires urgent medical intervention and treatment
  • Advise your patients to seek medical attention if they experience a combination of symptoms of pain, tenderness, erythema, or swelling in the genital or perineal area, with fever or malaise
  • Discontinue JARDIANCE if Fournier’s gangrene is suspected
  • See section 4.4 of SmPC for further details

KA: ketoacidosis; SGLT2: sodium-glucose co-transporter-2 inhibitors; SU: sulphonylurea; T2D: type 2 diabetes mellitus; UTI: urinary tract infection.

Learn more

JARDIANCE® (empagliflozin) clinical trial

Clinical trial

JARDIANCE® (empagliflozin) was studied in a dedicated CKD SGLT2 inhibitor trial published in The New England Journal of Medicine.3
JARDIANCE® (empagliflozin) efficacy

Efficacy

For your patients with CKD: help to reduce the risk of kidney disease progression or CV death in a broad patient population* vs placebo.1,3
JARDIANCE® (empagliflozin) initiation and management guide

JARDIANCE Initiation & Management guide for T2D, CHF and CKD

Key considerations when initiating or managing your patient with chronic kidney disease on JARDIANCE.

* EMPA-KIDNEY included patients with a wide range of underlying causes of CKD, many with co-morbidities across the spectrum of cardiovascular, kidney, or metabolic conditions. EMPA-KIDNEY included adult patients with an eGFR ≥20 to <45mL/min/1.73m2 or an eGFR ≥45 to <90mL/min/1.73m2 with a UACR ≥200mg/g, at risk of CKD progression.

Kidney disease progression defined as: adults with kidney function loss (sustained reduction of ≥40% eGFR decline, sustained eGFR <10mL/min/1.73m2), end stage kidney disease (initiation of chronic dialysis or kidney transplant), or renal death.

Abbreviations

CHF: chronic heart failure; CKD: chronic kidney failure; CV: cardiovascular; CVD: cardiovascular disease; T2D: type 2 diabetes mellitus.

References
  1. JARDIANCE® (empagliflozin) Summary of Product Characteristics (SmPC). Available at: http://www.medicines.org.uk/emc/medicine/28973.
  2. Kohler S, et al. 2017;34(7):1707-1726.
  3. Herrington WG, et al. N Engl J Med. 2023;388(2):117-127. (EMPA-KIDNEY results and the publication’s Supplementary Appendix).

PC-GB-108942 V2

March 2024

Reporting adverse events

Adverse events should be reported. Reporting form and information can be found at www.mhra.gov.uk/yellowcard. Adverse events should also be reported to Boehringer Ingelheim Drug Safety on 0800 328 1627 (freephone).

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