Associated Press WASHINGTON Sept. 3, 2004 â ProHeart 6, a twice-a-year time-released heartworm medication used to prevent the parasite in millions of dogs, was recalled Friday at the request of the Food and Drug Administration after thousands of animals suffered adverse reactions. ProHeart 6 was the first, and only, product approved by the FDA to be administered once every six months to treat heartworm disease in dogs. Its active ingredient, moxidectin, has been administered without problem to horses and cattle. The time-released version caused few problems when given to dogs at higher doses in clinical trials. Health and safety problems quickly cropped up, however, when ProHeart 6 was used to treat dogs after receiving FDA approval. As of Aug. 4, the drug agency received 5,552 reports of adverse reactions after dogs received heartworm shots. About 500 dogs died, though the agency said many deaths were not directly attributable to the product, manufactured by Fort Dodge Animal Health, based in Overland Park, Kan., a subsidiary of the pharmaceutical company Wyeth. Some dog deaths were linked convincingly to the heartworm medication, which prompted the recall, said Stephen F. Sundlof, director of the FDA's Center for Veterinary Medicine. Dog owners were urged to consult veterinarians about other medications to prevent heartworm. The agency had already asked Fort Dodge to revise the drug's label and to issue notices to veterinarians and dog owners pointing out safety questions associated with the product. "Despite all of the things that have been done, we continue to see these adverse events at approximately the same rate," Sundlof told reporters late Friday. The problems suffered by dogs include sudden lethargy, uncontrolled bleeding, vomiting, diarrhea, heart and liver problems and such nervous system abnormalities as seizures. "We don't really understand why this product is causing these problems," Sundlof said. "It affects dogs of all sizes and, apparently, dogs of all ages."