Follicle stimulating hormone/ganirelix Disease Interactions
There are 5 disease interactions with follicle stimulating hormone / ganirelix.
Follicle stimulating hormone (applies to follicle stimulating hormone/ganirelix) adrenal dysfunction
Major Potential Hazard, High plausibility. Applicable conditions: Adrenal Insufficiency, Hyperadrenocorticism
The use of follicle stimulating hormone (FSH) is contraindicated in patients with uncontrolled adrenal dysfunction. Uncontrolled adrenal dysfunction may involve the pituitary gland and be associated with a tumor or other dysfunction. Administration of FSH may exacerbate the condition.
References (4)
- "Product Information. Fertinex (urofollitropin)." Serono Laboratories Inc
- (2002) "Product Information. Follistim (follicle stimulating hormone)." Organon
- (2002) "Product Information. Gonal-F (follicle stimulating hormone)." Serono Laboratories Inc
- (2003) "Product Information. Bravelle (urofollitropin)." Ferring Pharmaceuticals Inc
Follicle stimulating hormone (applies to follicle stimulating hormone/ganirelix) thyroid dysfunction
Major Potential Hazard, Moderate plausibility. Applicable conditions: Hypothyroidism, Hyperthyroidism
The use of follicle stimulating hormone (FSH) is contraindicated in patients with uncontrolled thyroid dysfunction. FSH is composed of both an alpha and beta subunit. The amino acid sequence of the alpha subunit of FSH is identical to that of TSH. Therefore, FSH may have weak TSH receptor- binding and activation.
References (4)
- "Product Information. Fertinex (urofollitropin)." Serono Laboratories Inc
- (2002) "Product Information. Follistim (follicle stimulating hormone)." Organon
- (2002) "Product Information. Gonal-F (follicle stimulating hormone)." Serono Laboratories Inc
- (2003) "Product Information. Bravelle (urofollitropin)." Ferring Pharmaceuticals Inc
Follicle stimulating hormone (applies to follicle stimulating hormone/ganirelix) tumors
Major Potential Hazard, High plausibility. Applicable conditions: Neoplasia -- Estrogen Dependent
The use of follicle stimulating hormone is contraindicated in patients with sex hormone-dependent tumors of the reproductive tract and accessory organs (ovary, breast, uterus) and in patients with pituitary tumors. FSH is required for normal sex hormone production, which may be detrimental in these patients. Patients in later reproductive life have a greater predisposition to endometrial carcinoma.
References (4)
- "Product Information. Fertinex (urofollitropin)." Serono Laboratories Inc
- (2002) "Product Information. Follistim (follicle stimulating hormone)." Organon
- (2002) "Product Information. Gonal-F (follicle stimulating hormone)." Serono Laboratories Inc
- (2003) "Product Information. Bravelle (urofollitropin)." Ferring Pharmaceuticals Inc
Ganirelix (applies to follicle stimulating hormone/ganirelix) severe allergies
Major Potential Hazard, Moderate plausibility.
Treatment with ganirelix is not advised in women with severe allergic conditions.
References (1)
- (2001) "Product Information. Antagon (ganirelix)." Organon
Ganirelix (applies to follicle stimulating hormone/ganirelix) renal/hepatic impairment
Moderate Potential Hazard, Moderate plausibility. Applicable conditions: Liver Disease, Renal Dysfunction
The pharmacokinetics of ganirelix acetate injection have not been determined in special populations such as renally impaired and hepatically impaired patients. Caution is advised.
References (1)
- (2001) "Product Information. Antagon (ganirelix)." Organon
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Follicle stimulating hormone/ganirelix drug interactions
There are 7 drug interactions with follicle stimulating hormone / ganirelix.
More about follicle stimulating hormone / ganirelix
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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