Can you take CellCept with SourceCF ABDEK?
1 drug interaction and 8 additional warnings found for the following 2 drugs:
- CellCept (mycophenolate mofetil)
- SourceCF ABDEK (multivitamin with minerals)
Drug interactions
Minor drug interactions
Minor:
multivitamins with minerals mycophenolate mofetil
Applies to: SourceCF ABDEK (multivitamin with minerals) and CellCept (mycophenolate mofetil)
Information for this minor interaction is available on the professional version.
Food/lifestyle interactions
No alcohol/food interactions were found. However, this does not necessarily mean no interactions exist. Always consult your healthcare provider.
Disease interactions
8 potential interactions Applies to: 8 conditions, including Inflammatory Bowel Disease, Peptic Ulcer, Liver Disease, Neutropenia, and Renal Dysfunction.
Gastrointestinal Hemorrhage
Moderate:
CellCept
The mycophenolate mofetil in CellCept has a moderate potential interaction with Gastrointestinal Hemorrhage.
Gastrointestinal, rectal, and duodenal hemorrhage, hemorrhagic pancreatitis and rarely, large-intestine perforation have occurred in patients receiving mycophenolate. These events occurred primarily at dosages of mycophenolate >2 grams per day. Therapy with mycophenolate should be administered cautiously in patients with active gastrointestinal disease.
Inflammatory Bowel Disease
Moderate:
CellCept
The mycophenolate mofetil in CellCept has a moderate potential interaction with Inflammatory Bowel Disease.
Gastrointestinal, rectal, and duodenal hemorrhage, hemorrhagic pancreatitis and rarely, large-intestine perforation have occurred in patients receiving mycophenolate. These events occurred primarily at dosages of mycophenolate >2 grams per day. Therapy with mycophenolate should be administered cautiously in patients with active gastrointestinal disease.
Lesch-Nyhan Syndrome
Moderate:
CellCept
The mycophenolate mofetil in CellCept has a moderate potential interaction with Lesch-Nyhan Syndrome.
Mycophenolate mofetil is an inosine monophosphate dehydrogenase (IMPDH) inhibitor; therefore it should be avoided in patients with hereditary deficiencies of hypoxanthine-guanine phosphoribosyl-transferase (HGPRT) such as Lesch-Nyhan and Kelley-Seegmiller syndromes because it may cause an exacerbation of disease symptoms characterized by the overproduction and accumulation of uric acid leading to symptoms associated with gout such as acute arthritis, tophi, nephrolithiasis or urolithiasis and renal disease including renal failure.
Liver Disease
Moderate:
CellCept
The mycophenolate mofetil in CellCept has a moderate potential interaction with Liver Disease.
Mycophenolate mofetil (inactive) undergoes complete presystemic metabolism to active MPA , further metabolism to inactive forms, some of which undergo enterohepatic circulation producing a second peak of MPA. Alcoholic cirrhosis (parenchymal cell damage) does not appear to affect the metabolism of MPA to inactive forms. Hepatic disease/dysfunction due to other etiologies may induce different effects.
Neutropenia
Major:
CellCept
The mycophenolate mofetil in CellCept has a major potential interaction with Neutropenia.
Severe neutropenia has occurred in up to 2% of patients administered mycophenolate. Therapy with mycophenolate should be administered cautiously in patients with or predisposed to neutropenia. Mycophenolate should be discontinued or the dose reduced in patients who develop neutropenia (absolute neutrophil count <1300/mm3). Clinical monitoring of hematopoietic function is recommended. Complete blood counts should be performed weekly during the first month, two times a month during the second and third months, and monthly for the remainder of the first year of treatment.
Peptic Ulcer
Moderate:
CellCept
The mycophenolate mofetil in CellCept has a moderate potential interaction with Peptic Ulcer.
Gastrointestinal, rectal, and duodenal hemorrhage, hemorrhagic pancreatitis and rarely, large-intestine perforation have occurred in patients receiving mycophenolate. These events occurred primarily at dosages of mycophenolate >2 grams per day. Therapy with mycophenolate should be administered cautiously in patients with active gastrointestinal disease.
Renal Dysfunction
Moderate:
CellCept
The mycophenolate mofetil in CellCept has a moderate potential interaction with Renal Dysfunction.
Mycophenolate undergoes complete presystemic metabolism to its active form, MPA . Less than 1% of MPA is excreted in the urine. In a single-dose study, the area under the curve (AUC) for MPA in patients with severe chronic renal impairment (creatinine clearance <25 mL/min) was approximately 75% greater than those of healthy volunteers (creatinine clearance >80 mL/min). The AUC for the inactive metabolite was 3 to 6 times higher. Multiple dose studies have not been performed. No data are available for cardiac transplant patients with severe renal impairment and when benefit outweighs risk, therapy with mycophenolate should be administered with extreme caution.
Vaccination
Moderate:
CellCept
The mycophenolate mofetil in CellCept has a moderate potential interaction with Vaccination.
During treatment with mycophenolate mofetil, the use of live attenuated vaccines should be avoided and patients should be advised that vaccinations may be less effective. Advise patients to discuss with the physician before seeking any immunizations.
More resources
CellCept
A total of 365 drugs are known to interact with CellCept.
- Cellcept is in the drug class selective immunosuppressants.
- Cellcept is used to treat Organ Transplant, Rejection Prophylaxis.
SourceCF ABDEK
A total of 112 drugs are known to interact with SourceCF ABDEK.
- Sourcecf abdek is in the drug class vitamin and mineral combinations.
- Sourcecf abdek is used to treat Vitamin/Mineral Supplementation and Deficiency.
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
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.