Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Fidaxomicin
Drug ID BADD_D00896
Description Fidaxomicin is a novel macrolide antibiotic used in the treatment of diarrhea caused by _Clostridioides_ (formerly _Clostridium_) _difficile_ in adult and pediatric patients over the age of 6 months.[L11575] Fidaxomicin is a naturally-occurring 18-member macrocycle derived from fermentation.[A190501] Because fidaxomicin contains an 18-membered lactone ring in its structure, it is referred to as a macrocyclic lactone antibiotic drug.[A190492] The antibacterial activity of fidaxomicin is distinct from macrolides and rifamycins, as the bactericidal activity is time-dependent, and not concentration-dependent.[A190492] Fidaxomicin was the first macrocyclic lactone antibiotic with activity against _C. difficile_,[A190486] and it displays a narrow spectrum of activity against gram-positive anaerobes.[A7445] It mediates its potent bactericidal action on the bacteria by inhibiting the bacterial RNA synthase, thereby disrupting bacterial transcription.[A190486] The minimum inhibitory concentration (MIC90) for fidaxomicin is four times less than that of [vancomycin], which was the primary drug of choice for _C. difficile_ infection before the approval of fidaxomicin.[A190492] Unlike vancomycin, however, fidaxomicin has a negligible effect on normal colonic microflora.[A190516] The FDA initially approved fidaxomicin in May 2011 for the treatment of _C. difficile_-associated diarrhea in adult patients over the age of 18.[A190492] Later that year in December, the drug was also approved by the European Medicine Agency.[A190492] In June 2012, fidaxomicin was also granted approval by Health Canada.[A190486] The approved indication of fidaxomicin was expanded by the FDA in January 2020 to include pediatric patients over the age of 6 months in the treatment population.[L11575]
Indications and Usage Fidaxomicin is indicated for the treatment of _Clostridioides_ (formerly _Clostridium_) _difficile_-associated diarrhea in adult and pediatric patients 6 months of age and older.[L11575] Fidaxomicin should only be used in patients with proven or strongly suspected _C. difficile_ infection to reduce the risk of development of drug-resistant bacteria and maximize the therapeutic effectiveness of fidaxomicin and other antimicrobial agents.[L11575]
Marketing Status approved
ATC Code A07AA12
DrugBank ID DB08874
KEGG ID D09394
MeSH ID D000077732
PubChem ID 151383
TTD Drug ID D06LNW
NDC Product Code 52015-080; 65727-027; 62227-003; 52015-700; 55500-0007
UNII Z5N076G8YQ
Synonyms Fidaxomicin | Lipiarmycin A3 | Lipiarmycin | Tiacumicin B | PAR 101 | PAR101 | PAR-101 | Dificid | Lipiarmycin B4 | Tiacumicin C | Lipiarmycin B | Lipiarmycin A4 | Lipiarmycin B3
Chemical Information
Molecular Formula C52H74Cl2O18
CAS Registry Number 873857-62-6
SMILES CCC1C=C(C(CC=CC=C(C(=O)OC(CC=C(C=C(C1OC2C(C(C(C(O2)(C)C)OC(=O)C(C)C)O)O)C)C)C(C) O)COC3C(C(C(C(O3)C)OC(=O)C4=C(C(=C(C(=C4O)Cl)O)Cl)CC)O)OC)O)C
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Gastrointestinal pain07.01.05.005--
Haematochezia24.07.02.012; 07.12.02.0030.000270%Not Available
Hallucination, visual19.10.04.0070.000174%Not Available
Headache17.14.01.001--
Hepatocellular injury09.01.07.0080.000079%Not Available
Hyperglycaemia14.06.02.002; 05.06.02.002--
Hypersensitivity10.01.03.003--
Immune system disorder10.02.01.001--Not Available
Insomnia19.02.01.002; 17.15.03.0020.000309%
Intestinal obstruction07.13.01.002--Not Available
Megacolon07.02.05.002--Not Available
Melaena24.07.02.013; 07.12.02.0040.000079%Not Available
Metabolic acidosis14.01.01.003--Not Available
Mucous stools07.01.03.0060.000270%Not Available
Muscle spasms15.05.03.0040.000174%
Nausea07.01.07.0010.000737%
Nervous system disorder17.02.10.001--Not Available
Neutropenia01.02.03.004--Not Available
Platelet count decreased13.01.04.001--
Pruritus23.03.12.0010.000388%
Pyrexia08.05.02.0030.000293%
Rash23.03.13.001--Not Available
Rash maculo-papular23.03.13.0040.000174%
Skin disorder23.03.03.007--Not Available
Tachycardia02.03.02.0070.000174%Not Available
Urticaria23.04.02.001; 10.01.06.0010.000484%
Vomiting07.01.07.0030.000159%
Lymphatic disorder01.09.01.003--Not Available
Blood alkaline phosphatase increased13.04.02.004--
Hepatic enzyme increased13.03.04.028--Not Available
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