Tegison Disease Interactions
There are 4 disease interactions with Tegison (etretinate).
Retinoids (applies to Tegison) intracranial hypertension
Major Potential Hazard, High plausibility.
The use of retinoids has been associated with cases of pseudotumor cerebri (benign intracranial hypertension). Early signs and symptoms include papilledema, headache, nausea and vomiting, and visual disturbances. Patients who experience symptoms of this disorder while on retinoid therapy should be referred to a neurologist. If the diagnosis is confirmed, the retinoid should be discontinued permanently.
References (2)
- (2001) "Product Information. Accutane (isotretinoin)." Roche Laboratories
- (2001) "Product Information. Soriatane (acitretin)." Roche Laboratories
Retinoids (applies to Tegison) psychiatric disorders
Major Potential Hazard, Low plausibility. Applicable conditions: Psychosis, Depression
The use of retinoids, primarily isotretinoin, has been associated with causing depression, psychosis and rarely, suicidal ideation. Therapy with retinoids should be administered cautiously in patients with preexisting psychiatric conditions or depression. In addition to withdrawal of therapy, evaluation and follow-up may be necessary in affected patients.
References (2)
- (2001) "Product Information. Accutane (isotretinoin)." Roche Laboratories
- (2001) "Product Information. Soriatane (acitretin)." Roche Laboratories
Retinoids (applies to Tegison) elevated serum triglycerides
Moderate Potential Hazard, High plausibility. Applicable conditions: Obesity, Diabetes Mellitus, Alcoholism, Hyperlipidemia
The use of retinoids is associated with elevations in serum triglycerides and cholesterol, and decreases in HDL. In addition to cardiovascular risks, elevation of serum triglycerides to greater than 800 mg/dL has been associated with fatal fulminant pancreatitis. Patients at increased risk for developing hypertriglyceridemia during retinoid therapy include those with diabetes mellitus, obesity, high alcohol consumption, or a family history of these conditions. Blood lipid determinations should be performed prior to initiation of therapy and at 1- to 2- week intervals until the lipid response to the drug is established (usually 4 to 8 weeks). Patients with preexisting hyperlipidemia may require closer monitoring during retinoid therapy, and adjustments made accordingly in their lipid-lowering regimen.
References (1)
- (2001) "Product Information. Accutane (isotretinoin)." Roche Laboratories
Retinoids (applies to Tegison) liver disease
Moderate Potential Hazard, High plausibility.
The use of retinoids has been associated with elevations in liver enzymes and toxic hepatitis. Therapy with retinoids should be administered cautiously in patients with liver disease. Monitoring liver enzymes is recommended in these patients.
References (2)
- (2001) "Product Information. Accutane (isotretinoin)." Roche Laboratories
- (2001) "Product Information. Soriatane (acitretin)." Roche Laboratories
Switch to consumer interaction data
Tegison drug interactions
There are 59 drug interactions with Tegison (etretinate).
Tegison alcohol/food interactions
There are 2 alcohol/food interactions with Tegison (etretinate).
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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