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Infuvite Adult Pharmacy Bulk Package

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Infuvite Adult Pharmacy Bulk Package

Side Effects


The following adverse reactions are discussed in greater detail in other section of the labeling.

  • Allergic and anaphylactoid reactions following intravenous administration of thiamine [see WARNINGS AND PRECAUTIONS].
  • Hypervitaminosis A [see WARNINGS AND PRECAUTIONS]
Other adverse reactions

Dermatologic: rash, erythema, pruritis CNS: headache, dizziness, agitation, anxiety Ophthalmic : diplopia

Read the Infuvite Adult Pharmacy Bulk Package (multiple vitamins for infusion) Side Effects Center for a complete guide to possible side effects


A number of interactions between vitamins and drugs have been reported. Consult appropriate references for additional specific vitamin-drug interactions. The following are examples of these types of interactions:

Clinical interactions affecting levels of co-administered drugs

Folic Acid

Phenytoin metabolism may be increased by folic acid. Folic acid may lower the serum concentration of phenytoin resulting in increased seizure activity.

Patient's response to methotrexate therapy may be decreased by folic acid.


The metabolism of levodopa may be increased and its efficacy may be decreased by pyridoxine.


Antibiotic activity of erythromycin, kanamycin, streptomycin, doxycycline, and lincomycin is decreased by thiamine, riboflavin, pyridoxine, niacinamide, and ascorbic acid. Bleomycin is inactivated in vitro by ascorbic acid and riboflavin.

Clinical interactions affecting vitamin levels

Hydralazine, Isoniazid

Pyridoxine requirements may be increased by concomitant administration of hydralazine or isoniazid.


In patients with pernicious anemia, the hematologic response to vitamin B12 therapy may be inhibited by concomitant administration of chloramphenicol.


Serum folic acid concentrations may be decreased by phenytoin and, therefore it should be avoided in pregnancy.

This monograph has been modified to include the generic and brand name in many instances.

Last reviewed on RxList: 12/17/2012

Side Effects

Report Problems to the Food and Drug Administration


You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

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