Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Nabumetone
Drug ID BADD_D01511
Description Nabumetone was originally developed as a non-acidic non-steroidal anti-inflammatory drug (NSAID).[label] It was thought to avoid trapping of the drug in the stomach by making it unable to dissociate into ions which was believed to reduce GI toxicity by limiting local action.[A179077] While slightly reduced, possibly due to a degree of cyclooxygenase-2 selectivity (COX-2), nabumetone still produces significant adverse effects in the GI tract.[label,A178903] The molecule itself is a pro-drug with its 6-methoxy-2-naphthylacetic acid (6-MNA) metabolite acting as a potent COX inhibitor similar in structure to [naproxen]. Nabumetone was developed by Smithkline Beecham under the trade name Relafen and first received FDA approval in December, 1991.[L6568]
Indications and Usage **Indicated** for:[label] 1) Symptomatic relief in rheumatoid arthritis. 2) Symptomatic relief in osteoarthritis.
Marketing Status approved
ATC Code M01AX01
DrugBank ID DB00461
KEGG ID D00425
MeSH ID D000077430
PubChem ID 4409
TTD Drug ID D05CKR
NDC Product Code 49706-0681; 62331-008; 45865-464; 50090-6167; 60760-369; 60760-386; 62135-145; 0591-3671; 80425-0054; 65977-0082; 50228-465; 51655-733; 62135-146; 63629-8508; 69097-966; 72189-184; 76282-257; 15370-170; 69097-965; 71205-978; 71335-1234; 72189-072; 55700-845; 76420-210; 24196-135; 60687-630; 60760-368; 63187-307; 63629-8506; 69367-241; 69367-242; 0591-3670; 79739-7077; 50090-5386; 50228-466; 53002-6960; 61919-668; 68788-7597; 68788-7765; 79739-7076; 80425-0104; 65015-632; 43063-972; 45865-111; 50090-5294; 51655-446; 60760-387; 63187-378; 63629-7699; 63629-8509; 71335-1272; 71335-1391; 45865-997; 55700-840; 61919-609; 71335-1559; 63629-8510; 76282-258; 80425-0053; 63187-484; 71205-030; 71205-530; 71205-977; 72789-040; 79739-7078
UNII LW0TIW155Z
Synonyms Nabumetone | Nabumeton | 4-(6-Methoxy-2-naphthyl)-2-butanone | Relifex | Relif | Apo-Nabumetone | ApoNabumetone | Mebutan | Listran | Gen-Nabumetone | Arthraxan | BRL 14777 | Rhoxal-nabumetone | Rhoxal nabumetone | Relafen | Nabucox
Chemical Information
Molecular Formula C15H16O2
CAS Registry Number 42924-53-8
SMILES CC(=O)CCC1=CC2=C(C=C1)C=C(C=C2)OC
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)
Tension19.06.02.005--Not Available
Thrombocytopenia01.08.01.002--Not Available
Thrombophlebitis24.01.02.001--Not Available
Tinnitus17.04.07.004; 04.04.01.002--
Toxic epidermal necrolysis23.03.01.008; 12.03.01.015; 11.07.01.006; 10.01.01.006--
Tremor17.01.06.002--
Urticaria23.04.02.001; 10.01.06.0010.000468%
Vaginal haemorrhage24.07.03.005; 21.08.01.001--
Vasculitis24.12.04.027; 10.02.02.006--
Vertigo17.02.12.002; 04.04.01.003--
Visual impairment06.02.10.013--Not Available
Vomiting07.01.07.003--
Weight decreased13.15.01.005--
Weight increased13.15.01.006--
Tubulointerstitial nephritis20.05.02.0020.000347%Not Available
Hypoacusis04.02.01.0060.000173%
Acute coronary syndrome24.04.04.011; 02.02.02.015--Not Available
Haemorrhage24.07.01.002--Not Available
Decreased appetite14.03.01.005; 08.01.09.028--
Erectile dysfunction21.03.01.007; 19.08.04.001--
Ill-defined disorder08.01.03.049--Not Available
Occult blood positive13.05.02.001--Not Available
Nephritic syndrome20.05.01.006--Not Available
Acute kidney injury20.01.03.0160.000867%
Liver function test increased13.03.04.031--Not Available
Hypersensitivity pneumonitis22.01.01.027; 10.01.03.056--Not Available
Renal cell carcinoma stage III20.01.04.025; 16.08.02.0150.000173%Not Available
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ADReCS-Target
Drug Name ADR Term Target
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