Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Plerixafor
Drug ID BADD_D01788
Description Plerixafor is a hematopoietic stem cell mobilizer. It is used to stimulate the release of stem cells from the bone marrow into the blood in patients with non-Hodgkin lymphoma and multiple myeloma for the purpose of stimulating the immune system. These stem cells are then collected and used in autologous stem cell transplantation to replace blood-forming cells that were destroyed by chemotherapy. Plerixafor has orphan drug status in the United States and European Union; it was approved by the U.S. Food and Drug Administration on December 15, 2008.
Indications and Usage Used in combination with granulocyte-colony stimulating factor (G-CSF, filgrastim) to mobilize hematopoietic stem cells to the peripheral blood for collection and subsequent autologous transplantation in patients with non-Hodgkin’s lymphoma (NHL) and multiple myeloma (MM).
Marketing Status Prescription
ATC Code L03AX16
DrugBank ID DB06809
KEGG ID D08971
MeSH ID C088327
PubChem ID 65015
TTD Drug ID D0L5RW
NDC Product Code 54893-0050; 68554-0067; 55111-954; 76055-0017; 42973-202; 71924-0063; 0024-5862
Synonyms plerixafor | 1,1'-(1,4-phenylenebis-(methylene))-bis-1,4,8,11-tetraazacyclotetradecane | plerixafor octahydrochloride | mezobil | mozobil | JM3100 | JM 3100 | AMD 3100 | AMD-3100 | AMD3100 | plerixafor hydrochloride | RPA bicyclam | AMD 3329 | AMD-3329 | plerixafor octahydrobromide | 1,1'-(1,4-phenylenebis-(methylene))-bis-1,4,8,11-tetraazacyclotetradecane octahydrochloride dihydrate | 1,1'-(1,4-phenylenebis(methylene))bis(1,4,8,11-tetraazacyclotetradecane)octahydrochloride dihydrate
Chemical Information
Molecular Formula C28H54N8
CAS Registry Number 110078-46-1
SMILES C1CNCCNCCCN(CCNC1)CC2=CC=C(C=C2)CN3CCCNCCNCCCNCC3
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Abdominal discomfort07.01.06.001--Not Available
Abdominal distension07.01.04.001--
Abdominal pain07.01.05.002--
Abnormal dreams19.02.03.001; 17.15.02.001--Not Available
Anaphylactic reaction24.06.03.006; 10.01.07.001--
Anaphylactic shock24.06.02.004; 10.01.07.0020.005146%Not Available
Arthralgia15.01.02.001--
Blood pressure decreased13.14.03.0020.019727%Not Available
Chest pain02.02.02.011; 22.02.08.003; 08.01.08.0020.029590%Not Available
Chills15.05.03.016; 08.01.09.0010.019727%
Confusional state19.13.01.001; 17.02.03.0050.019727%
Constipation07.02.02.001--
Death08.04.01.001--
Diarrhoea07.02.01.0010.039453%
Dizziness24.06.02.007; 17.02.05.003; 02.01.02.004--
Dry mouth07.06.01.002--
Dyspepsia07.01.02.001--
Dyspnoea22.02.01.004; 02.01.03.0020.019727%
Erythema23.03.06.0010.019727%Not Available
Fatigue08.01.01.002--
Flatulence07.01.04.002--
Haematoma24.07.01.001--
Hallucination19.10.02.0020.029590%
Headache17.14.01.001--
Hyperhidrosis23.02.03.004; 08.01.03.028--
Hypersensitivity10.01.03.0030.029590%
Hypokalaemia14.05.03.0020.029590%
Injection site reaction08.02.03.014; 12.07.03.015--
Insomnia19.02.01.002; 17.15.03.0020.019727%
Malaise08.01.01.0030.019727%
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