Pet Drug Reports

Ingredients

Active ingredient · pooled across combinations

Chlortetracycline Calcium Complex: adverse event reports, pooled

2 ingredient sets in reports · 9 FDA-approved applications in the Green Book

89reports naming the ingredient, 2012–20240% of all reports · about 6 a year
0reports, 12 months to March 20262 in the 12 months before
74.6%classed serious, as reportedall reports: 38.6%
70.8%of reports concern cattlehorse 2.2%

89 adverse event reports received by FDA list a drug containing chlortetracycline calcium complex, alone or in combination, from April 2012 to October 2024. This page pools every ingredient set that includes it; 2 such sets appear in reports.

The Green Book lists 9 FDA-approved applications containing it. openFDA masks brand and manufacturer names in adverse event records, so the reports counted here cannot be attributed to a particular brand.

0 reports arrived in the 12 months to March 2026, against 2 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. That is about 6 reports a year over its reporting history and 0% of all reports.

Pooled across every set, the terms listed most often are death (42.7%), lack of efficacy - NOS (40.4%) and ineffective, antibiotic (16.9%). Many drugs combine several ingredients, and many reports list several drugs, so a term on this page may relate to any of them or to none.

Of reports that state seriousness, 74.6% were classed as serious (38.6% across the whole database); 49.4% record a death or euthanasia (6.4% overall). Ingredients used in older or sicker animals, or in anaesthesia and cancer care, carry higher shares for that reason alone.

Ingredient sets that include chlortetracycline calcium complex

Active ingredients recorded for the drugReportsShare of this page's reportsLatest 12 months
Chlortetracycline Calcium Complex7988.8%0
Chlortetracycline Calcium Complex + Sulfamethazine1112.4%0

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"; counts follow sales volume and years on the market. A report can list more than one set, so shares can add to more than 100%.

Signs listed in reports, pooled

share of chlortetracycline calcium complex reports listing the termall reports in the database

  1. Death42.7%38
  2. Lack of efficacy - NOS[the product did not have the expected effect]40.4%36
  3. Ineffective, antibiotic[legacy FDA term: the product did not have the expected effect (antibiotic)]16.9%15
  4. Color, Abnormal[a product quality report, not a sign in an animal]5.6%5
  5. Containers, Damaged[a product quality report, not a sign in an animal]4.5%4
  6. Appearance, Abnormal[a product quality report, not a sign in an animal]3.4%3
  7. Closure, Abnormal[a product quality report, not a sign in an animal]3.4%3
  8. Death by euthanasia[the animal was euthanized]3.4%3
  9. Lack of efficacy (bacteria) - NOS[the product did not have the expected effect: target not specified]3.4%3
  10. No sign[no clinical sign was reported]2.2%2
  11. Odor, Abnormal[a product quality report, not a sign in an animal]2.2%2
  12. Underdose[less than the labelled amount was given]2.2%2
  13. Anorexia[not eating]1.1%1
  14. Atrial fibrillation1.1%1
  15. Closure, Missing[a product quality report, not a sign in an animal]1.1%1
  16. Containers, Abnormal[a product quality report, not a sign in an animal]1.1%1
  17. Containers, Leaking[a product quality report, not a sign in an animal]1.1%1
  18. Contamination NOS[NOS: not otherwise specified]1.1%1
  19. Contamination, Insects1.1%1
  20. Elevated lactate1.1%1
  21. Hard, clumping[a product quality report, not a sign in an animal]1.1%1
  22. Lack of efficacy (bacteria NOS)[the product did not have the expected effect: bacteria NOS]1.1%1
  23. Lack of efficacy (protozoa) - Coccidia[the product did not have the expected effect: coccidia]1.1%1

Pooled across every ingredient set and every report that names the ingredient. One report can list several terms and several drugs; a term here may relate to any of them or to none.

Monthly reports by species, five years

Dog0 · peak 1
2022202320242025
Cat0 · peak 1
2022202320242025
Horse2 · peak 2
Feb 2023: 22022202320242025
Other26 · peak 5
Jul 2021: 3Sep 2021: 2Oct 2021: 1Nov 2021: 5Feb 2022: 1Apr 2022: 1Jun 2022: 1Jul 2022: 1Sep 2022: 1Nov 2022: 1Dec 2022: 1Feb 2023: 2May 2023: 2Jan 2024: 1Feb 2024: 1Aug 2024: 1Oct 2024: 12022202320242025

By month of receipt; each panel has its own scale. The newest months are incomplete because FDA posts reports with a delay of three to six months.

08162012: 420122013: 520132017: 920172018: 1020182019: 1520192020: 1620202021: 1320212022: 720222023: 620232024: 42024

Outcomes, report types and ages

Outcome recorded in the report

Recovered/Normal9%8
Recovered with Sequela3.4%3
Ongoing5.6%5
Died47.2%42
Euthanized4.5%4
Outcome Unknown47.2%42

What kind of report it was

Safety issue14.6%13
Lack of expected effectiveness57.3%51
Both safety and lack of expected effectiveness3.4%3
Manufacturing or product defect24.7%22
Other0%0

Species

Cattle70.8%63
Horse2.2%2
Chicken1.1%1
Pig1.1%1

Age of the animal

Under 1 year19.1%17
1 to 3 years7.9%7
4 to 7 years0%0
8 to 11 years1.1%1
12 years and over0%0
Age not given71.9%64

Coloured bar: reports naming chlortetracycline calcium complex. Grey bar: all 1,357,245 reports. Outcomes are as stated by the reporter; FDA has not necessarily determined whether any product played a part.

In context

MeasureChlortetracycline Calcium ComplexAll reports
Reports891,357,245
Latest 12 months against the 12 before-100%-5%
Classed serious, of reports stating it74.6%38.6%
Death or euthanasia recorded, per 1,000 reports494.463.8
Filed as lack of expected effectiveness (wholly or partly)60.7%23%

Shares of reports, not of animals treated: how many animals receive the ingredient is not public. Ingredients used in anaesthesia, cancer care or in old animals carry more serious outcomes in their reports for that reason alone.

FDA-approved products containing chlortetracycline calcium complex (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.

Trade nameActive ingredientsSponsorApproved forApplication
PfiChlor 50; PfiChlor 70; PfiChlor 100Chlortetracycline Calcium ComplexPhibro Animal Health Corp.Cattle, Swine, Chickens, Turkeys, SheepNADA 049-287
Cltc 10; Cltc 20; Cltc 30; Cltc 50; Cltc 70Chlortetracycline Calcium ComplexPhibro Animal Health Corp.Cattle, Swine, Chickens, Turkeys, SheepNADA 092-286
Aureomycin / SacoxChlortetracycline Calcium Complex, Salinomycin SodiumHuvepharma EOODChickensANADA 200-095
Chlorachel 250 Swine; Pficlor 1000; Pficlor 250; Pficlor-SP 250approval voluntarily withdrawnChlortetracycline Calcium Complex, Penicillin G Procaine, SulfamethazineZoetis Inc.SwineNADA 091-668
Chlorachel 10; Chlorachel 20; Chlorachel 35approval voluntarily withdrawnChlortetracycline Calcium ComplexPfizer, Inc.—NADA 100-903
Aureomycin / Cygroapproval voluntarily withdrawnChlortetracycline Calcium Complex, Maduramicin AmmoniumAmerican Cyanamid, Division AHP Corp.—NADA 140-837
Aureomycin / Bio-Cox / 3-Nitroapproval voluntarily withdrawnChlortetracycline Calcium Complex, Roxarsone, Salinomycin SodiumZoetis Inc.ChickensNADA 140-867
3-Nitro / Aureomycin / Sacoxapproval voluntarily withdrawnChlortetracycline Calcium Complex, Roxarsone, Salinomycin SodiumHuvepharma EOODChickensANADA 200-091
Aureozol 500 Granularapproval voluntarily withdrawnChlortetracycline Calcium Complex, Penicillin G Procaine, SulfathiazoleZoetis Inc.SwineANADA 200-167

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 chlortetracycline calcium complex reports

How many FDA adverse event reports mention chlortetracycline calcium complex?

89 reports through March 2026, 0 of them in the latest 12 months, counting chlortetracycline calcium complex alone and in combinations.

Which brands 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. The Green Book reference list on this page names approved products containing chlortetracycline calcium complex without any counts.

In which combinations is chlortetracycline calcium complex reported?

Chlortetracycline Calcium Complex (88.8% of these reports) and Chlortetracycline Calcium Complex + Sulfamethazine (12.4% of these reports).

What reactions are reported for chlortetracycline calcium complex?

death (42.7%), lack of efficacy - NOS (40.4%), ineffective, antibiotic (16.9%), color, Abnormal (5.6%) and containers, Damaged (4.5%). Shares are of reports naming the ingredient; one report can list several terms.

Which animals are these reports about?

cattle (70.8%), horse (2.2%) and chicken (1.1%).

Does a high count mean chlortetracycline calcium complex is a problem ingredient?

A count 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." Widely used ingredients collect more reports because more animals receive them.

How do I report a problem?

Call the drug company using the number on the label, or send Form FDA 1932a to FDA. 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. Ingredient names follow the Green Book; salts and forms are kept as FDA lists them. Drug entries are matched by the active ingredients their unmasked ingredient field discloses. 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.