Drugs by active ingredient › Estradiol + Tylosin Tartrate
Drug · combination of 2 active ingredients
Estradiol + Tylosin Tartrate: adverse event reports
All products with this ingredient combination · no approved product with exactly this set
- Mostly cattle reports
- Other route most often
- Brands masked by FDA
Between April 2012 and June 2024 FDA received 74 adverse event reports listing a drug with the combination estradiol and tylosin tartrate as the recorded active ingredients. No FDA-approved product has exactly this set of ingredients; the ingredient field of a report can be incomplete.
openFDA masks the brand and manufacturer in every report, so these figures describe the ingredient combination across all products and cannot be attributed to a brand.
In the 12 months to March 2026, 0 reports named it, against 1 in the 12 months before. Recent months are provisional: fDA posts reports quarterly with a delay of three to six months, so the newest months are incomplete and usually grow in later releases. Over its whole reporting history that is about 5 reports a year and 0% of all 1,357,245 reports (0.2% of all cattle reports). How many animals received it is not published, so a count says nothing about how often a problem occurs per dose.
The signs named most often are death (50%), unclassifiable adverse event (28.4%) and behavioural disorder NOS (27%). A report can list several signs, so shares add to more than 100%; 93 different terms appear across these reports. Death appears in 50% of these reports, a larger share than in the pooled reports for every drug containing tylosin tartrate (11.4%).
89.2% of reports concern cattle. Not every report describes illness: 10.8% as product or packaging defects. Of reports that state seriousness, 27.3% were classed as serious, and 58.1% of all reports record a death or euthanasia as an outcome, as reported. FDA has not necessarily determined whether any drug played a part.
Monthly reports by species, five years
Reports by the month FDA received them. Each panel has its own scale; the peak month is printed at the top right. The newest months are incomplete because FDA posts reports with a delay of three to six months.
Reports by year received
2024 covers reports received through March 2026 only.
Signs listed in reports
share of estradiol + tylosin tartrate reports listing the termall drugs containing tylosin tartrateall cattle reports
- Death50%37
- Unclassifiable adverse event[event that fits no dictionary term]28.4%21
- Behavioural disorder NOS[behaviour change, type not specified]27%20
- Respiratory tract disorder NOS[NOS: not otherwise specified]21.6%16
- Pneumonia[lung infection or inflammation]18.9%14
- Lameness17.6%13
- Digestive tract disorder NOS[digestive problem, type not specified]16.2%12
- Peritonitis[inflamed abdominal lining]8.1%6
- Bloated6.8%5
- Musculoskeletal disorder NOS[NOS: not otherwise specified]6.8%5
- Respiratory signs6.8%5
- Reticulitis6.8%5
- Weight gain6.8%5
- Abscess NOS[NOS: not otherwise specified]5.4%4
- Aggression5.4%4
- Flatulence, bloating and distension5.4%4
- Liver failure5.4%4
- Nasal discharge5.4%4
- Ruminal bloat5.4%4
- Systemic disorder NOS[NOS: not otherwise specified]5.4%4
- Trauma NOS[NOS: not otherwise specified]5.4%4
- Acute (interstitial) pneumonia/pleuropneumonia4.1%3
- Claw / hoof / nail disorder NOS[NOS: not otherwise specified]4.1%3
- Death by euthanasia[the animal was euthanized]4.1%3
- Hypersalivation[drooling]4.1%3
- Loss of condition4.1%3
- NT - Abnormal necropsy finding NOS[NOS: not otherwise specified]4.1%3
- Product Defect, General[a product quality report, not a sign in an animal]4.1%3
- Pulmonary fibrosis4.1%3
Top 30 of 93 coded terms (VeDDRA, the veterinary reporting dictionary; plain-language gloss in brackets). One report can list several terms. The ticks show how often the same term appears in a wider pool of reports; they describe the reports, and FDA cautions that such figures cannot be used to estimate risk or to compare one product with another. openFDA masks brand and manufacturer names in adverse event records, so the reports counted here cannot be attributed to a particular brand.
Outcomes and report types
Outcome recorded in the report
What kind of report it was
Coloured bar: reports naming estradiol + tylosin tartrate. Grey bar: all 1,357,245 reports in the database. Outcomes are the status at the time of the last report, as stated by the reporter; a report covering several animals can carry more than one outcome. FDA has not necessarily determined whether any drug played a part in any outcome.
Species and breeds in the reports
Species
Single-breed animals
Breed shares follow how common each breed is. Crossbred animals and reports with no breed stay in the species figure only.
Age, weight and route
Age of the animal
Weight of the animal
Route of administration stated in reports: other (36), subcutaneous (7), parenteral (2), cutaneous (1).
In context
| Measure | Estradiol + Tylosin Tartrate | All drugs containing tylosin tartrate | All cattle reports | All reports |
|---|---|---|---|---|
| Reports | 74 | 621 | 31,229 | 1,357,245 |
| Share of that pool's reports naming this drug | — | 11.9% | 0.2% | 0% |
| Classed serious, of reports stating it | 27.3% | 26% | 58.4% | 38.6% |
| Death or euthanasia recorded, per 1,000 reports | 581.1 | 145 | 368 | 63.8 |
| Filed as lack of expected effectiveness (wholly or partly) | 4.1% | — | — | 23% |
| Top term, share of reports | Death 50% | 11.4% | 29.4% | — |
The tylosin tartrate pool is every report naming tylosin tartrate alone or in any combination; this combination accounts for 11.9% of it. Shares are of reports, not of animals treated. The number of doses sold is not public, so none of these figures is a rate of occurrence, and differences between columns reflect which animals receive a drug and who reports as much as anything else.
Other ingredient sets sharing an ingredient
| Active ingredients | Reports | Latest 12 months |
|---|---|---|
| Tylosin Tartrate | 513 | 31 |
| Estradiol | 428 | 11 |
| Estradiol + Trenbolone Acetate | 267 | 16 |
| Estradiol + Testosterone | 47 | 0 |
| Estradiol + Norgestomet | 44 | 0 |
| Estradiol + Trenbolone Acetate + Tylosin Tartrate | 31 | 4 |
Listed for navigation, ordered by report count. FDA states that these data "cannot be used to estimate the risk associated with the product or compare one drug or device product with another": drugs differ in formulation, in the animals they are given to, in sales volume and in years on the market. A report's ingredient field can be incomplete, so reports about one product may sit under more than one set.
FDA-approved products (Green Book)
Reference information, not report statistics. openFDA masks brand and manufacturer names in adverse event records, so the reports counted here cannot be attributed to a particular brand. The list below is the FDA Green Book as of 1 Oct 2026; nothing on this page says which of these products, if any, a report concerned.
No approved product has exactly this set of active ingredients. The ingredient field of a report can be incomplete; these approved products contain all of the ingredients named here, together with others.
| Trade name | Active ingredients | Sponsor | Approved for | Application |
|---|---|---|---|---|
| Component TE-G; Component TE-G with Tylan; Component TE-IS; Component TE-IS with Tylan; Component TE-S; Component TE-S with Tylan | Estradiol, Trenbolone Acetate, Tylosin Tartrate | Elanco US Inc. | Cattle | ANADA 200-221 |
| Component TE-200 with Tylan; Component TE-H with Tylan; Component TE-IH with Tylan | Estradiol, Trenbolone Acetate, Tylosin Tartrate | Elanco US Inc. | Cattle | ANADA 200-346 |
Species are the major species the Green Book search lists for the application ("—" where it lists another species or none). Approval dates are not part of the Green Book listing files and are not shown. Pioneer applications (NADA) come first, then generics (ANADA).
Questions about estradiol + tylosin tartrate reports
How many adverse event reports has FDA received for the combination estradiol and tylosin tartrate?
74 reports record a drug with the combination estradiol and tylosin tartrate as its active ingredients in the openFDA release of 28 Sep 2026, covering reports received through March 2026. 0 of them arrived in the latest 12 months.
Which brand do these reports concern?
That cannot be known from the public data. openFDA masks brand and manufacturer names in adverse event records, so the reports counted here cannot be attributed to a particular brand.
What signs are reported most often?
death (50%), unclassifiable adverse event (28.4%), behavioural disorder NOS (27%), respiratory tract disorder NOS (21.6%) and pneumonia (18.9%). These are the coded terms listed in reports; several can appear in one report, and a term's presence is not a finding that the drug was responsible.
Which species and breeds appear in these reports?
cattle (89.2%). Among single-breed animals the most frequent labels are Holstein-Friesian, Charolais, French Black Pied Holstein-Friesian and Maine-Anjou; popular breeds appear often in any drug's reports because there are more of them.
Are reports rising?
0 reports in the 12 months to March 2026, against 1 in the 12 months before. FDA posts reports quarterly with a delay of three to six months, so the newest months are incomplete and usually grow in later releases. Counts also move with sales, publicity and time on the market.
Do these reports show that estradiol + tylosin tartrate harms pets?
Report counts cannot show that. FDA states that "there is no certainty that the reported drug or device caused the adverse event" and that the event "may have been related to an underlying disease, other drugs used at the same time or other non-drug related sources." FDA also notes that commonly used products may have more reports simply because more animals receive them.
Are these the side effects of estradiol + tylosin tartrate?
They are signs listed in reports, not an established list of side effects. The adverse reactions observed in studies are printed on each product's FDA-approved label, which a veterinarian can go through with you. This page is a record of what was reported to FDA.
How do I report a problem with an animal drug?
FDA asks owners and veterinarians to call the drug company first (the number is on the label); companies must pass reports to FDA. Reports can also go directly to FDA on Form FDA 1932a. See the guide on how to report.
Where this comes from. Counts are built from the openFDA Animal & Veterinary adverse event bulk files released 28 Sep 2026, which hold reports FDA's Center for Veterinary Medicine received through 31 Mar 2026. openFDA masks brand and manufacturer names in these files, so drugs are counted by the active ingredients each record discloses and no figure is attributed to a brand, application or company. Ingredient names, and the separate reference lists of approved products, follow the FDA Green Book as of 1 Oct 2026. Drug entries are grouped by the active ingredients their unmasked ingredient field discloses; the application number that records also carry is not used. No report text, lot numbers or reporter details are published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.