FOLLTROPIN<sup>®</sup> <br/>[porcine pituitary-derived follicle stimulating hormone for injection]
Folltropin Follicle Stimulating Hormone (Porcine) Folltropin Follicle Stimulating Hormone (Porcine) Follicle Stimulating Hormone (Porcine) Follitropin Sterile Diluent Bacteriostatic sodium chloride Sodium Chloride Benzyl Alcohol Water
NADA 141-431, Approved by FDA CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.
DESCRIPTION: FOLLTROPIN® (porcine pituitary-derived follicle stimulating hormone for injection) is a powder for solution containing 700 IU (equivalent to 400 mg NIH-FSH-P1) of follicle stimulating hormone (FSH) per vial. FOLLTROPIN® contains a low amount of luteinizing hormone (less than 1000 µg NIH-LH-S19 per vial). When reconstituted according to label directions the final solution contains 35 IU FSH per mL for intramuscular injection. There are no inactive ingredients in the FSH vial. A 20 mL vial of sterile diluent for FOLLTROPIN® is supplied containing 9 mg/mL sodium chloride, 18 mg/mL benzyl alcohol, sodium hydroxide in sufficient quantity to adjust pH, and water for injection q.s.
INDICATIONS FOR USE: For the induction of superovulation in beef and dairy heifers and cows. Not for use in male cattle or reproductively immature heifers because safety and effectiveness have not been tested.
DOSAGE AND ADMINISTRATION: For intramuscular injection only. Reconstitute FOLLTROPIN® with 20 mL of the diluent provided using strict aseptic technique. Do not use if clumps or particles are visible after gentle mixing.
Regimen: Start injections on day 8 to 10 following observed or induced estrus. Administer 2.5 mL (87.5 IU) of FOLLTROPIN® intramuscularly, twice daily at 12 hour intervals, for 4 consecutive days. In conjunction with the 6th dose of FOLLTROPIN®, administer an FDA-approved prostaglandin product (cloprostenol sodium or dinoprost tromethamine) for cattle, using the labeled dosage and administration instructions to cause luteolysis and induce estrus. Inseminate animals at 12 and 24 hours after the onset of estrus or 60 and 72 hours after prostaglandin treatment. Additional inseminations may be conducted at 12 hour intervals, if indicated. Collection of embryos is normally started on day 7 following insemination.
CONTRAINDICATIONS: Do not use in pregnant cattle. Laboratory studies with FSH in rats and rabbits have shown evidence of embryotoxicity/fetotoxicity and the safety of the product has not been assessed in pregnant cows. Do not use FOLLTROPIN® in cows that are known to be hypersensitive to the active ingredient, porcine pituitary-derived follicle stimulating hormone.
WARNINGS AND PRECAUTIONS:
Withdrawal Period:
Withdrawal Period
Neither a withdrawal period nor a milk discard time is required when this product is used according to label directions.
User Safety Warnings: Not for use in humans. Keep out of reach of children. Care should be taken when handling the product to avoid accidental self-injection. Accidental self-injection may cause biological effects in women and, if pregnant, to the unborn child. In the event of accidental self-injection seek medical attention immediately by consulting a physician/health professional, particularly in women who are pregnant, or whose pregnancy status is unknown. To obtain a Safety Data Sheet or to report adverse reactions, contact 1-800-835-9496 and make this number available to the physician/health professional.
Animal Safety Warnings and Precautions: Management considerations: Successful use of FOLLTROPIN® depends on good reproductive health of the cow and quality herd management procedures. Cattle should be clinically healthy and cycling normally. A comprehensive and ongoing nutritional, reproductive, and herd health program should be in place when using FOLLTROPIN® for superovulation. The use of this product may result in trim loss of edible tissue at slaughter.
ADVERSE REACTIONS: Following superovulation, a delayed return to heat is possible. Use of this product has been associated with a low incidence of hypersensitivity or anaphylactic reactions. If you notice any serious effects or other effects not mentioned in this leaflet, please inform your veterinarian.
TARGET ANIMAL SAFETY: Existing pharmacology and toxicology information and knowledge gained from the widespread clinical use of FOLLTROPIN® in cattle was sufficient to demonstrate that FOLLTROPIN® is not systemically toxic to the cow and the targets of toxicity in both cattle and other species are limited to the reproductive organs and functions. A field safety study demonstrated that the use of FOLLTROPIN® in accordance with label directions did not produce any reactions at the injection site. A retrospective study of dairy cattle superovulated up to six times at intervals of less than 93 days did not show any adverse effect of repeated superovulation on the yield of transferable embryos. Cows within the superovulation program produced embryos that were successfully transferred into recipient cows and were able to themselves conceive and deliver normal calves. The development of cystic ovaries following treatment with FOLLTROPIN® has been reported; however, these results have not been substantiated by well-controlled studies or through a comprehensive literature review.
EFFECTIVENESS: The effectiveness of FOLLTROPIN® for the induction of superovulation in beef and dairy heifers and cows was substantiated through a systematic review and meta-analysis which included 2685 superovulation records obtained from twenty clinical studies and one retrospective study. The analysis revealed a high level of variability in the number of transferable embryos obtained between treatment groups; such variability is representative of the expected variation for superovulation programs. The estimated mean number of transferable embryos was 4.5 per study animal and the 95% confidence limits of the mean were 3.5 (lower limit) and 5.6 (upper limit).
STORAGE, HANDLING, AND DISPOSAL: Freeze-dried powder and diluent vials: Do not store above 25°C (77°F). Reconstituted solution: Store under refrigeration (2 to 8 °C; 36 to 46°F). Keep the vials in the outer carton in order to protect from light. Shelf life following reconstitution according to directions: 4 days Do not freeze after reconstitution. Discard any unused portion of the reconstituted FOLLTROPIN® solution. See FDA's website http://www.fda.gov/safesharpsdisposal for information on safe disposal of needles and other sharps. Unless otherwise directed, dispose of unused medicine and empty containers in solid waste following applicable Federal, State and local environmental laws and regulations.
HOW SUPPLIED: FOLLTROPIN® contains one 20 mL vial containing 700 IUIU = International Units (established by WHO Expert Committee on Biological Standardization in 1986). FSH as a lyophilized powder and one 20 mL diluent vial containing Bacteriostatic Sodium Chloride.
CONTACT INFORMATION: Contact Vétoquinol USA, Inc. at 1-800-267-5707 for customer service or to obtain product information, including a SDS. After hours or to report adverse reactions, call 1-800-835-9496. For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS or online at http://www.fda.gov/AnimalVeterinary/SafetyHealth.
Made in Canada
Distributed by:
Vétoquinol USA, Inc.
4250 N. Sylvania Ave.
Ft. Worth, TX (USA) 76137
www.vetoquinolusa.com
PRINCIPAL DISPLAY PANEL - Kit Carton FOLLTROPIN ®
[Porcine Pituitary-Derived Follicle
Stimulating Hormone for Injection] INJECTABLE SOLUTION For use in beef and dairy
heifers and cows only. CAUTION: Federal law restricts this drug to use by or on the order
of a licensed veterinarian. Net Contents:
One 20 mL vial containing 700 IU FSH as a lyophilized powder
One 20 mL diluent vial containing Bacteriostatic Sodium Chloride vetoquinoL NDC 17030 101 70
NADA 141-431, Approved by FDA PRINCIPAL DISPLAY PANEL - Kit Carton