Tilmicosin Phosphate (Micotil 300, Pulmotil 90): adverse event reports that FDA received
Active ingredient
Also sold as: Micotil 300, Pulmotil 90, Tilmovet AC.
The openFDA records give the value "MSK" for the brand name and for the manufacturer name of each drug. FDA says that MSK means "masked". So the site cannot count a report for a brand.
Read this first. FDA says this about the data:
An API dataset query result cannot be used to estimate the risk associated with the product or compare one drug or device product with another. When looking at the results, be aware that there is no certainty that the reported drug or device caused the adverse event. This dataset should not be the sole source of information for clinical decision-making or other assumptions about the safety or effectiveness of a product. The adverse event may have been related to an underlying disease, other drugs used at the same time or other non-drug related sources.
FDA Center for Veterinary Medicine publishes these words. Source: Adverse Event Reports for Animal Drugs and Devices, read on . The data have the reports that FDA received through .
This page is not veterinary advice. For an animal that is ill, speak to a veterinarian.
Contacting a veterinarianHow to report to FDAFrom May 1992 to April 2025, FDA received 3,573 adverse event reports that name a drug with tilmicosin phosphate as its active ingredient. Of the 3,573 reports, 2,274 (63.6%) are about people who were exposed to the drug. 827 reports are about cattle (23.1%).
In January to March 2026, FDA received no reports that name this drug. The signs that appear in the largest number of the 3,573 reports are "Accidental exposure", "Unclassifiable adverse event" and "Death". A report is not proof that a drug caused a sign.
Fewer than 20 reports named this drug in the 12 months before June 2026, so this page gives no change. Reports about people who were exposed to the drug are 63.6% of the reports that name this drug, and 1.2% of all reports.
Search engines list a drug page with 500 reports or more in all years. The page also needs 30 reports or more in the 12 months to June 2026. This page is under one of these numbers. The site keeps the page and keeps it out of search engines.
Since the last update of the FDA data
The latest update of the FDA data, recorded on , changed no count of this page.
January to March 2026 is the latest closed quarter in the data. In that quarter FDA received 0 reports that name tilmicosin phosphate: 0 dog, 0 cat, 0 horse, 0 other or not given.
Signs that the reports list
A sign is a coded term from the report. The words in brackets are a plain gloss of the term. The percentage is the share of the 3,573 reports that list the sign. One report can list more than one sign.
The sign that is in the largest number of the reports comes first.
- Accidental exposure[exposure that was not intended]61.6%2,202 reports
- Unclassifiable adverse event[event that fits no dictionary term]58.6%2,095 reports
- Death20.1%718 reports
- No sign[no clinical sign was reported]18.4%659 reports
- Injection site pain[pain where the injection was given]7.7%275 reports
- Injection site swelling[swelling where the injection was given]6.7%241 reports
- Lack of efficacy (bacteria) - NOS[the product did not have the expected effect: target not specified]6.5%232 reports
- Sensory abnormality NOS[NOS: not otherwise specified]6.5%232 reports
- Injection site bleeding[bleeding where the injection was given]6.1%217 reports
- Nausea4.1%146 reports
- Balance problem3.9%141 reports
- Collapse3.7%131 reports
- Tachycardia[fast heart rate]3.6%130 reports
- Hypoaesthesia3.5%124 reports
Show the next 16 signs
- Injection site inflammation[inflammation where the injection was given]3.1%111 reports
- Headache3.1%109 reports
- Dyspnoea[difficulty breathing]3%107 reports
- Recumbency[lying down and unable or unwilling to rise]2.9%103 reports
- Thoracic pain2.5%89 reports
- Anxious state of mind2.3%81 reports
- Anaphylaxis[sudden severe allergic-type reaction]2%70 reports
- Hypertension[high blood pressure]2%70 reports
- Weakness1.9%67 reports
- Fever1.8%64 reports
- Vomiting1.8%64 reports
- Anorexia[not eating]1.7%60 reports
- Accidental drug intake by child1.7%59 reports
- Feeling depressed1.4%51 reports
- Musculoskeletal pain1.4%49 reports
- Lameness1.2%44 reports
The list shows 30 of 523 coded signs. A report is not proof that a drug caused a sign. Download all signs (CSV)
Reports by species
The share is of all 3,573 reports that name tilmicosin phosphate. The other reports give a different species or no species.
Reports for each month, Jul 2021 to Jun 2026
No chart: no month has 5 or more reports.
No chart: no month has 5 or more reports.
No chart: no month has 5 or more reports.
No chart: no month has 5 or more reports.
The month is the month in which FDA received the report. Each chart has its own scale. FDA says that a report can take 3 to 6 months to reach the public data. The newest months can get more reports in a later update.
Reports by year
- Dog
- Cat
- Horse
- Other or not given
| Year | Dog | Cat | Horse | Other or not given | All species |
|---|---|---|---|---|---|
| 2025 | 0 | 0 | 0 | 1 | 1 |
| 2024 | 0 | 0 | 0 | 1 | 1 |
| 2023 | 0 | 0 | 0 | 1 | 1 |
| 2022 | 0 | 0 | 0 | 1 | 1 |
| 2020 | 0 | 0 | 0 | 3 | 3 |
| 2015 | 0 | 0 | 0 | 33 | 33 |
| 2014 | 0 | 0 | 0 | 60 | 60 |
| 2013 | 1 | 0 | 0 | 44 | 45 |
| 2012 | 0 | 0 | 0 | 71 | 71 |
| 2011 | 0 | 0 | 0 | 83 | 83 |
| 2010 | 0 | 0 | 0 | 69 | 69 |
| 2009 | 2 | 0 | 0 | 105 | 107 |
| 2008 | 0 | 0 | 0 | 69 | 69 |
| 2007 | 1 | 0 | 1 | 179 | 181 |
| 2006 | 2 | 0 | 0 | 178 | 180 |
| 2005 | 1 | 1 | 0 | 283 | 285 |
| 2004 | 0 | 0 | 0 | 287 | 287 |
| 2003 | 2 | 0 | 1 | 390 | 393 |
| 2002 | 0 | 2 | 2 | 275 | 279 |
| 2001 | 0 | 0 | 1 | 241 | 242 |
| 2000 | 0 | 0 | 0 | 224 | 224 |
| 1999 | 0 | 0 | 0 | 311 | 311 |
| 1998 | 0 | 0 | 0 | 101 | 101 |
| 1997 | 1 | 1 | 0 | 113 | 115 |
| 1996 | 1 | 0 | 0 | 82 | 83 |
| 1995 | 0 | 0 | 0 | 93 | 93 |
| 1994 | 0 | 0 | 0 | 104 | 104 |
| 1993 | 0 | 0 | 0 | 84 | 84 |
| 1992 | 1 | 0 | 0 | 66 | 67 |
2025 has the reports that FDA received through Apr 2025. Download the years (CSV)
What the reports record
Outcome at the time of the report
- Recovered/Normal3.6%128
- Recovered with Sequela[recovered, with a lasting effect]0.4%15
- Ongoing0%0
- Died23.3%834
- Euthanized0.1%5
- Outcome Unknown1.9%67
An outcome in a report is not proof that the drug caused it. The person who sends the report gives the outcome. Each share is of the 3,573 reports that name tilmicosin phosphate.
A report about more than one animal can have more than one outcome.
Kind of report
- Safety issue96.4%3,446
- Lack of expected effectiveness0.2%8
- Both safety and lack of expected effectiveness0.5%18
- Manufacturing or product defect2.8%101
- Other0%0
254 reports say if the event was serious. 53.5% of them have the serious flag. The person who sends the report sets the flag.
Show age, weight, breed and route
Age of the animal
- Under 1 year12.9%460
- 1 to 3 years3.8%134
- 4 to 7 years1%37
- 8 to 11 years0.4%15
- 12 years and over54.6%1,950
- Age not given27.3%977
Weight of the animal
- Under 5 kg (11 lb)0.6%22
- 5 to 9.9 kg (11 to 22 lb)1%35
- 10 to 24.9 kg (22 to 55 lb)2.2%79
- 25 to 44.9 kg (55 to 99 lb)2%73
- 45 kg and over (99 lb and over)21.6%771
- Weight not given72.6%2,593
Breed, where the report gives one breed
- Holstein-Friesian3.2%114
- Aberdeen Angus1.7%60
- Charolais0.6%20
- Simmental0.3%10
- Pygmy0.3%9
- Nubian0.2%8
- Suffolk sheep0.2%8
- Limousin0.2%7
A breed with many animals has many reports.
Route in the report
- Intramuscular32.9%1,174
- Subcutaneous21.7%774
- Oral14.5%519
- Topical8.1%290
- Other5.8%206
- Ophthalmic1.3%48
Each bar is on a scale of 0 to 100%.
Approved animal drugs with this active ingredient (FDA Green Book)
This section is reference data. It has no report count.
The openFDA records give the value "MSK" for the brand name and for the manufacturer name of each drug. FDA says that MSK means "masked". So the site cannot count a report for a brand.
Brand names
- Micotil 300
- Pulmotil 90
- Tilmovet AC
What the Green Book records give
- Applications with an approval in force
- 3
- Approved species
- Cattle, Swine, Sheep
- Dose forms
- Aqueous Concentrate, Liquid, Type A Medicated Article
- Routes
- Oral, Oral, in drinking water, Subcutaneous
- Sale
- RX (prescription), VFD (veterinary feed directive)
- Earliest approval date in the records
The species, dose forms and routes are the words of the Green Book records for all the applications together. One product can have fewer. The label of a product gives its approved use.
| Brand name | Active ingredients | Sponsor | Approved species | Application |
|---|---|---|---|---|
| Micotil 300 | Tilmicosin Phosphate | Elanco US Inc. | Cattle, Sheep | NADA 140-929 |
| Pulmotil 90 | Tilmicosin Phosphate | Elanco US Inc. | Cattle, Swine | NADA 141-064 |
| Tilmovet AC | Tilmicosin Phosphate | Huvepharma EOOD | Swine | ANADA 200-707 |
Next in the A to Z list
FDA pages for this drug
- How to Report Animal Drug and Device Side Effects and Product ProblemsThe FDA page that tells an owner or a veterinarian how to send a report.
- Green Book record of NADA 140-929The FDA record of the application for Micotil 300.
- Green Book record of NADA 141-064The FDA record of the application for Pulmotil 90.
- Green Book record of ANADA 200-707The FDA record of the application for Tilmovet AC.
- Animal Drugs @ FDAThe search page of the Green Book, the FDA list of approved animal drugs.
The site checked these addresses on . The links open in a new tab.
Cite this page
Pet Drug Reports. Tilmicosin Phosphate: adverse event reports that FDA received. https://petdrugreports.com/drug/tilmicosin-phosphate/ Source: FDA Center for Veterinary Medicine, openFDA Animal and Veterinary adverse event reports, export of . Reports received through .
Where the data come from
The counts come from the openFDA Animal and Veterinary adverse event files, export of 30 Oct 2026. The files have the reports that the FDA Center for Veterinary Medicine received through 26 Jun 2026. The files mask brand and manufacturer names. The site counts a drug by the active ingredients that each record gives, and gives no count to a brand, an application or a company. Ingredient names and the lists of approved products follow the FDA Green Book of 2 Nov 2026. The site does not use the application number that a record has.
The site does not publish report text, lot numbers or details of a reporter. FDA's record is the authority. See how the site counts reports, the data sources and the corrections page.
Questions about these reports
- Which brand are these reports about?
The openFDA records give the value "MSK" for the brand name and for the manufacturer name of each drug. FDA says that MSK means "masked". So the site cannot count a report for a brand. The Green Book section of this page lists the brand names with this active ingredient.
- Do the reports show that the drug caused the signs?
No. FDA states this about the data.
When looking at the results, be aware that there is no certainty that the reported drug or device caused the adverse event.
The adverse event may have been related to an underlying disease, other drugs used at the same time or other non-drug related sources.
FDA Center for Veterinary Medicine. Source: Adverse Event Reports for Animal Drugs and Devices
- How many reports did FDA receive in the latest 12 months?
FDA received no reports in the 12 months to June 2026. It received 1 report in the 12 months before. FDA says that a report can take 3 to 6 months to reach the public data. The newest months can get more reports in a later update.
- What kinds of report are in the count?
Of the 3,573 reports received from May 1992 to April 2025, 96.4% are about a safety issue only. 0.7% are about a lack of expected effectiveness, alone or with a safety issue. 2.8% are about a defect of the product or its package.