Parenteral Manual

Tigecycline (NON-FORMULARY)

Disclaimer: Official controlled document is the CHEO online copy. It is the responsibility of user to ensure that any paper copy version is the same as the online version before use.

Alternate Name(s): 
TYGACIL
Classification: 
Glycylcycline Antibiotic
Original Date: 
April 2008
Revised Date: 
September 2011
Indications: 
  • Treatment of complicated skin and skin structure infections caused by susceptible organisms
    (includes gram positive, gram-negative and anaerobes)
  • Treatment of complicated intra-abdominal infections
Reconstitution and Stability: 
VIAL SIZE 0.9% NaCl or D5W REQUIRED FINAL CONCENTRATION
50 mg 5.3 mL 10 mg/mL
  • Gently swirl to dissolve  - immediately withdraw dose from vial and further dilute
  • Diluted solution stable 6 hours at room temperature or 24 hours in fridge
  • Reconstituted solution should be yellow-orange in colour;  if not,discard
Compatibility: 

-Solutions Compatible:  D5W, 0.9% NaCl, ringer's lactate

-Additives/Above Cassette Compatible:  no information

-Y-site Compatible:  amikacin, dobutamine, dopamine, gentamicin, lidocaine, morphine, norepinephrine, piperacillin/tazobactam, potassium chloride, propofol, ranitidine,  tobramycin

-Incompatible:  amphotericin B, chlorpromazine, methylprednisolone, voriconazole

Administration: 

(For approved routes of administration by nursing personnel, refer to Policy for the Administration of Intravenous Medications.)

SC NO
IM NO
IV Direct NO
IV Intermittent Infusion YES
Usual dilution: in 100 mL minibag of NS 
Infusion time: over 30 - 60 minutes
IV Continuous Infusion NO
Dosage: 

(For neonatal dosages, refer to Neonatal IV Drug Manual.)

Pediatric:

  • safety & efficacy not established in children

Adolescent / Adult:

  • 100 mg IV  initial dose, then 50 mg IV Q12H for 5 to 14 days
  • No dosage adjustment required for renal impairment or after hemodialysis
  • No dosage adjustment required for mild to moderate hepatiac impairment
  • For severe  hepatic impairment:   100 mg IV  initial dose then 25 mg IV Q12H
Potential hazards of parenteral administration: 
  • Most common:  nausea, vomiting, diarrhea
  • Local reactions at the IV infusion site:  edema, pain
  • Hypersensitivity reactions
Notes: 
  • Monitor INR when used concomitantly with warfarin -  decreased clearance of warfarin
  • Structurally similar to tetracycline-  therefore, not recommended for use in children<8 or in pregnancy.  Permanent discoloration of the teeth may occur if used during tooth development.

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