Expanded broad-spectrum IV antibiotic indicated for adults with
cSSSI, cIAI, and CABP due to the indicated pathogens*
(Please see Indications and Important Safety Information)
TYGACIL – the first glycylcycline – was designed to circumvent key bacterial resistance mechanisms1,16,19
- TYGACIL is unaffected by resistance mechanisms that have affected antibacterial
drug use1,15-18 - Ribosomal protections1,15,17,18
- Macrolide or tetracycline efflux pumps1,15,17,18
- PBP alterations (target site modifications) 1,17,18
- Beta-lactamases (including extended-spectrum beta-lactamases)1,16
- DNA gyrase mutations1,17
- Tigecycline resistance in some bacteria (eg, Acinetobacter calcoaceticus–Acinetobacter baumannii complex) is associated with multi-drug resistant (MDR) efflux pumps1
TYGACIL binds to the ribosome, thereby inhibiting protein synthesis1,15,19

Glycylcyclines overcome key mechanisms of resistance1,15-18
- Glycylcyclines bind to the ribosome with five times higher affinity than tetracycline15,16,19
- TYGACIL binds to additional sites of the ribosome in a manner not seen before, interfering with the mechanism of ribosomal protection proteins15,16
- TYGACIL is not expelled by macrolide or tetracycline efflux pumps1
TYGACIL Update
- TYGACIL is in the CMS/Joint Commission Quality Measures for non-ICU Bacterial CAP patients
Treatment Guidelines
- TYGACIL is in the IDSA guidelines for cIAI and SIS guidelines for cIAI and cSSSI5,6 Learn more about TYGACIL in Treatment Guidelines
Resistance Monitoring Data
The Tigecycline Evaluation and Surveillance Trial (T.E.S.T.) is a comprehensive global surveillance study
initiated in 2004 to evaluate the in vitro activity of tigecycline (TYGACIL) and commonly used antimicrobials
against gram-positive and -negative bacterial pathogens.
Find data on susceptibility to TYGACIL from isolates collected in the United States between 2004 and Present,
and learn more about resistance monitoring data
Indications and Important Safety Information
*Indications
TYGACIL® (tigecycline) is indicated for the treatment of adults with:
- Complicated skin and skin structure infections caused by Escherichia coli, Enterococcus faecalis (vancomycin-susceptible isolates), Staphylococcus aureus (methicillin-susceptible and -resistant isolates), Streptococcus agalactiae, Streptococcus anginosus grp. (includes S. anginosus, S. intermedius, and S. constellatus), Streptococcus pyogenes, Enterobacter cloacae, Klebsiella pneumoniae, and Bacteroides fragilis
- Complicated intra-abdominal infections caused by Citrobacter freundii, Enterobacter cloacae, Escherichia coli, Klebsiella oxytoca, Klebsiella pneumoniae, Enterococcus faecalis (vancomycin-susceptible isolates), Staphylococcus aureus (methicillin-susceptible and -resistant isolates), Streptococcus anginosus grp. (includes S. anginosus,
S. intermedius, and S. constellatus), Bacteroides fragilis, Bacteroides thetaiotaomicron, Bacteroides uniformis, Bacteroides vulgatus, Clostridium perfringens, and Peptostreptococcus micros - Community-acquired bacterial pneumonia caused by Streptococcus pneumoniae (penicillin-susceptible isolates), including cases with concurrent bacteremia, Haemophilus influenzae (beta-lactamase negative isolates), and Legionella pneumophila
Important Safety Information
- TYGACIL is contraindicated in patients with known hypersensitivity to tigecycline
- Anaphylaxis/anaphylactoid reactions have been reported with nearly all antibacterial agents, including tigecycline, and may be life-threatening. TYGACIL should be administered with caution in patients with known hypersensitivity to tetracycline-class antibiotics
- Isolated cases of significant hepatic dysfunction and hepatic failure have been reported in patients being treated with tigecycline. Some of these patients were receiving multiple concomitant medications. Patients who develop abnormal liver function tests during tigecycline therapy should be monitored for evidence of worsening hepatic function. Adverse events may occur after the drug has been discontinued
- The safety and efficacy of TYGACIL in patients with hospital-acquired pneumonia have not been established
- An increase in all-cause mortality has been observed across phase 3 and 4 clinical studies in TYGACIL-treated patients versus comparator-treated patients. The cause of this increase has not been established. This increase in all-cause mortality should be considered when selecting among treatment options
- TYGACIL may cause fetal harm when administered to a pregnant woman
- The use of TYGACIL during tooth development may cause permanent discoloration of the teeth. TYGACIL should not be used during tooth development unless other drugs are not likely to be effective or are contraindicated
- Acute pancreatitis, including fatal cases, has occurred in association with tigecycline treatment. Consideration should be given to the cessation of the treatment with tigecycline in cases suspected of having developed pancreatitis
- Clostridium difficile-associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents, including TYGACIL, and may range in severity from mild diarrhea to fatal colitis
- Monotherapy should be used with caution in patients with clinically apparent intestinal perforation
- TYGACIL is structurally similar to tetracycline-class antibiotics and may have similar adverse effects. Such effects may include: photosensitivity, pseudotumor cerebri, and anti-anabolic action (which has led to increased BUN, azotemia, acidosis, and hyperphosphatemia). As with tetracyclines, pancreatitis has been reported with the use of TYGACIL
- To reduce the development of drug-resistant bacteria and maintain the effectiveness of TYGACIL and other antibacterial drugs, TYGACIL should be used only to treat infections proven or strongly suspected to be caused by susceptible bacteria. As with other antibacterial drugs, use of TYGACIL may result in overgrowth of non-susceptible organisms, including fungi
- The most common adverse reactions (incidence >5%) are nausea, vomiting, diarrhea, infection, headache, and abdominal pain
- Prothrombin time or other suitable anticoagulant test should be monitored if TYGACIL is administered with warfarin
- Concurrent use of antibacterial drugs with oral contraceptives may render oral contraceptives less effective
- The safety and effectiveness of TYGACIL in patients below age 18 and lactating women have not been established
Please see full Prescribing Information.