Opdivo Qvantig Disease Interactions
There are 5 disease interactions with Opdivo Qvantig (hyaluronidase / nivolumab).
Nivolumab (applies to Opdivo Qvantig) hepatic impairment
Moderate Potential Hazard, Moderate plausibility. Applicable conditions: Liver Disease
There are no data available on the use of nivolumab-containing products in patients with severe hepatic impairment or autoimmune liver disease. No dose adjustment is recommended for patients with mild or moderate hepatic impairment during use of IV nivolumab; data not available for subcutaneous nivolumab. Monitor liver enzymes at baseline and periodically during therapy. Therapy with nivolumab-containing products may cause immune-mediated hepatitis and/or hepatotoxicity.
References (2)
- (2023) "Product Information. Opdivo (nivolumab)." Bristol-Myers Squibb, SUPPL-119
- (2024) "Product Information. Opdivo Qvantig (hyaluronidase-nivolumab)." Bristol-Myers Squibb
Nivolumab (applies to Opdivo Qvantig) pneumonitis
Moderate Potential Hazard, Moderate plausibility. Applicable conditions: Pleuropulmonary Infection, History - Radiation Therapy
Use of nivolumab-containing products can cause immune-mediated pneumonitis. The incidence of pneumonitis is higher in patients who have received prior thoracic radiation.
References (2)
- (2023) "Product Information. Opdivo (nivolumab)." Bristol-Myers Squibb, SUPPL-119
- (2024) "Product Information. Opdivo Qvantig (hyaluronidase-nivolumab)." Bristol-Myers Squibb
PD-1/PD-L1 inhibitors (applies to Opdivo Qvantig) HSCT
Moderate Potential Hazard, Moderate plausibility. Applicable conditions: Bone Marrow Transplantation
Fatal and other serious complications can occur in patients who receive allogeneic hematopoietic stem cell transplantation (HSCT) before or after being treated with a programmed death receptor-1/ligand-1 (PD-1/PD-L1) blocking antibody. Transplant-related complications include hyperacute graft-versus-host disease (GVHD), acute GVHD, chronic GVHD, hepatic veno-occlusive disease after reduced intensity conditioning, and steroid-requiring febrile syndrome (without an identified infectious cause). These complications may occur despite intervening therapy between PD-1/PD-L1 blockade and allogeneic HSCT. It is recommended to follow patients closely for evidence of transplant-related complications and intervene promptly. The benefit versus risks of treatment with a PD-1/PD-L1 blocking antibody before or after an allogeneic HSCT should be considered.
References (10)
- (2023) "Product Information. Opdivo (nivolumab)." Bristol-Myers Squibb, SUPPL-119
- (2023) "Product Information. Zynyz (retifanlimab)." Incyte Corporation
- (2023) "Product Information. Libtayo (cemiplimab)." Regeneron Pharmaceuticals Inc, SUPPL-16
- (2023) "Product Information. Jemperli (dostarlimab)." GlaxoSmithKline, SUPPL-6
- (2023) "Product Information. Tecentriq (atezolizumab)." Genentech, SUPPL-51
- (2022) "Product Information. Bavencio (avelumab)." EMD Serono Inc, SUPPL-13
- (2023) "Product Information. Imfinzi (durvalumab)." Astra-Zeneca Pharmaceuticals, SUPPL-42
- (2024) "Product Information. Keytruda (pembrolizumab)." Merck Sharp & Dohme LLC, SUPPL-160
- (2024) "Product Information. Tevimbra (tislelizumab)." BeiGene USA, Inc
- (2024) "Product Information. Opdivo Qvantig (hyaluronidase-nivolumab)." Bristol-Myers Squibb
PD-1/PD-L1 inhibitors (applies to Opdivo Qvantig) myasthenia gravis
Moderate Potential Hazard, Moderate plausibility.
Myasthenic syndrome/myasthenia gravis (including exacerbation) has been reported with the use of programmed death receptor-1/ligand-1 (PD-1/PD-L1) blocking antibodies. Care should be exercised when using PD-1/PD-L1 blocking antibodies in patients with myasthenia gravis.
References (9)
- (2023) "Product Information. Opdivo (nivolumab)." Bristol-Myers Squibb, SUPPL-119
- (2023) "Product Information. Zynyz (retifanlimab)." Incyte Corporation
- (2023) "Product Information. Libtayo (cemiplimab)." Regeneron Pharmaceuticals Inc, SUPPL-16
- (2023) "Product Information. Jemperli (dostarlimab)." GlaxoSmithKline, SUPPL-6
- (2023) "Product Information. Tecentriq (atezolizumab)." Genentech, SUPPL-51
- (2022) "Product Information. Bavencio (avelumab)." EMD Serono Inc, SUPPL-13
- (2023) "Product Information. Imfinzi (durvalumab)." Astra-Zeneca Pharmaceuticals, SUPPL-42
- (2024) "Product Information. Keytruda (pembrolizumab)." Merck Sharp & Dohme LLC, SUPPL-160
- (2024) "Product Information. Opdivo Qvantig (hyaluronidase-nivolumab)." Bristol-Myers Squibb
PD-1/PD-L1 inhibitors (applies to Opdivo Qvantig) organ transplant
Moderate Potential Hazard, Moderate plausibility.
Solid organ transplant rejection and other transplant (including corneal graft) rejection have been reported with the use of programmed death receptor-1/ligand-1 (PD-1/PD-L1) blocking antibodies. Care should be exercised when using PD-1/PD-L1 blocking antibodies in patients who have received a solid organ or other transplant.
References (10)
- (2023) "Product Information. Opdivo (nivolumab)." Bristol-Myers Squibb, SUPPL-119
- (2023) "Product Information. Zynyz (retifanlimab)." Incyte Corporation
- (2023) "Product Information. Libtayo (cemiplimab)." Regeneron Pharmaceuticals Inc, SUPPL-16
- (2023) "Product Information. Jemperli (dostarlimab)." GlaxoSmithKline, SUPPL-6
- (2023) "Product Information. Tecentriq (atezolizumab)." Genentech, SUPPL-51
- (2022) "Product Information. Bavencio (avelumab)." EMD Serono Inc, SUPPL-13
- (2023) "Product Information. Imfinzi (durvalumab)." Astra-Zeneca Pharmaceuticals, SUPPL-42
- (2024) "Product Information. Keytruda (pembrolizumab)." Merck Sharp & Dohme LLC, SUPPL-160
- (2024) "Product Information. Tevimbra (tislelizumab)." BeiGene USA, Inc
- (2024) "Product Information. Opdivo Qvantig (hyaluronidase-nivolumab)." Bristol-Myers Squibb
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Opdivo Qvantig drug interactions
There are 661 drug interactions with Opdivo Qvantig (hyaluronidase / nivolumab).
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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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