Solganal Disease Interactions
There are 8 disease interactions with Solganal (aurothioglucose).
- Bone marrow aplasia
- Congestive heart failure
- Diabetes mellitus
- Liver disease
- Rash
- Renal dysfunction
- Severe hypertension
- Systemic lupus erythematosus
Auranofin (applies to Solganal) bone marrow aplasia
Major Potential Hazard, High plausibility. Applicable conditions: Bone Marrow Depression/Low Blood Counts
The use of auranofin and other gold compounds is contraindicated in patients with a history of gold- induced bone marrow aplasia. Prior to gold compounds therapy, a complete blood count with a differential, platelet count, urinalysis, and renal and liver function tests should be performed. A complete blood count with a differential, platelet count, and urinalysis should be done at least monthly during therapy. Hematological warning signs of gold toxicity include a drop in hemoglobin, leukopenia (WBC < 4,000/mm3), granulocytopenia (< 1,500/mm3), and thrombocytopenia (<100,000/mm3).
References (3)
- (2001) "Product Information. Ridaura (auranofin)." SmithKline Beecham
- (2001) "Product Information. Solganal (aurothioglucose)." Schering Corporation
- (2022) "Product Information. Myochrysine (gold sodium thiomalate)." Merck & Co., Inc
Gold compounds (applies to Solganal) congestive heart failure
Major Potential Hazard, Moderate plausibility.
The use of gold compounds is contraindicated in patients with uncontrolled congestive heart failure. Prior to initiation of gold compounds medical problems that might affect the signs and symptoms used to detect gold compounds toxicity should be under control.
References (3)
- (2001) "Product Information. Ridaura (auranofin)." SmithKline Beecham
- (2001) "Product Information. Solganal (aurothioglucose)." Schering Corporation
- (2022) "Product Information. Myochrysine (gold sodium thiomalate)." Merck & Co., Inc
Gold compounds (applies to Solganal) diabetes mellitus
Major Potential Hazard, Low plausibility.
The use of gold compounds is contraindicated in patients with controlled diabetes mellitus.
References (3)
- (2001) "Product Information. Ridaura (auranofin)." SmithKline Beecham
- (2001) "Product Information. Solganal (aurothioglucose)." Schering Corporation
- (2022) "Product Information. Myochrysine (gold sodium thiomalate)." Merck & Co., Inc
Gold compounds (applies to Solganal) liver disease
Major Potential Hazard, High plausibility.
The use of gold compounds is contraindicated in patients with hepatic dysfunction. Prior to gold compounds therapy, a complete blood count with a differential, platelet count, urinalysis, and renal and liver function tests should be performed. A complete blood count with a differential, platelet count, and urinalysis should be done at least monthly during therapy.
References (3)
- (2001) "Product Information. Ridaura (auranofin)." SmithKline Beecham
- (2001) "Product Information. Solganal (aurothioglucose)." Schering Corporation
- (2022) "Product Information. Myochrysine (gold sodium thiomalate)." Merck & Co., Inc
Gold compounds (applies to Solganal) rash
Major Potential Hazard, High plausibility. Applicable conditions: Eczema
The use of gold compounds is contraindicated in patients with urticaria or eczema. Prior to initiation of gold therapy, medical problems that might affect the signs and symptoms used to detect gold toxicity should be under control.
References (3)
- (2001) "Product Information. Ridaura (auranofin)." SmithKline Beecham
- (2001) "Product Information. Solganal (aurothioglucose)." Schering Corporation
- (2022) "Product Information. Myochrysine (gold sodium thiomalate)." Merck & Co., Inc
Gold compounds (applies to Solganal) renal dysfunction
Major Potential Hazard, High plausibility.
The use of gold compounds is contraindicated in patients with chronic renal failure. These patients may be at increased risk for renal toxicity. Prior to gold compounds therapy, a complete blood count with a differential, platelet count, urinalysis, and renal and liver function tests should be performed. A complete blood count with a differential, platelet count, and urinalysis should be done at least monthly during therapy.
References (3)
- (2001) "Product Information. Ridaura (auranofin)." SmithKline Beecham
- (2001) "Product Information. Solganal (aurothioglucose)." Schering Corporation
- (2022) "Product Information. Myochrysine (gold sodium thiomalate)." Merck & Co., Inc
Gold compounds (applies to Solganal) severe hypertension
Major Potential Hazard, Moderate plausibility.
The use of gold compounds is contraindicated in patients with severe hypertension. Prior to initiation of gold compounds medical problems that might affect the signs and symptoms used to detect gold compounds toxicity should be under control.
References (3)
- (2001) "Product Information. Ridaura (auranofin)." SmithKline Beecham
- (2001) "Product Information. Solganal (aurothioglucose)." Schering Corporation
- (2022) "Product Information. Myochrysine (gold sodium thiomalate)." Merck & Co., Inc
Gold compounds (applies to Solganal) systemic lupus erythematosus
Major Potential Hazard, High plausibility.
The use of gold compounds is contraindicated in patients with systemic lupus erythematosus. Prior to gold compounds therapy, a complete blood count with a differential, platelet count, urinalysis, and renal and liver function tests should be performed. A complete blood count with a differential, platelet count, and urinalysis should be done at least monthly during therapy.
References (3)
- (2001) "Product Information. Ridaura (auranofin)." SmithKline Beecham
- (2001) "Product Information. Solganal (aurothioglucose)." Schering Corporation
- (2022) "Product Information. Myochrysine (gold sodium thiomalate)." Merck & Co., Inc
Switch to consumer interaction data
Solganal drug interactions
There are 153 drug interactions with Solganal (aurothioglucose).
Solganal alcohol/food interactions
There is 1 alcohol/food interaction with Solganal (aurothioglucose).
More about Solganal (aurothioglucose)
- Check interactions
- Compare alternatives
- Side effects
- Dosage information
- During pregnancy
- Drug class: antirheumatics
Related treatment guides
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. |
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Further information
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