Adverse Drug Reaction Classification System

         

Pharmaceutical Information
Drug Name Amoxicillin
Drug ID BADD_D00129
Description Amoxicillin, or BRL-2333, is a penicillin G derivative first described in the literature in 1972.[A190648] Amoxicillin has similar activity to [penicillin] and [ampicillin], but leads to higher serum concentrations than ampicillin.[A190648] Amoxicillin was granted FDA approval on 18 January 1974.[L11644]
Indications and Usage Amoxicillin alone is indicated to treat susceptible bacterial infections of the ear, nose, throat, genitourinary tract, skin, skin structure, and lower respiratory tract.[L11656,L11659] Amoxicillin is given with calvulanic acid to treat acute bacterial sinusitis, community acquired pneumonia, lower respiratory tract infections, acute bacterial otitis media, skin and skin structure infections, and urinary tract infections.[L11650,L7880,L11653] Amoxicillin is given with omeprazole in the treatment of _H. pylori_.[L9743,L11647]
Marketing Status approved; vet_approved
ATC Code J01CA04
DrugBank ID DB01060
KEGG ID D00229; D07452
MeSH ID D000658
PubChem ID 33613
TTD Drug ID D0F6EO
NDC Product Code 0781-5060; 55657-101; 55657-106; 59651-099; 65862-274; 0093-2268; 0093-4161; 43063-563; 0143-9886; 50090-0304; 50090-0858; 50090-1511; 50090-5863; 50090-5880; 51655-156; 53002-0130; 53002-2080; 55289-182; 57237-029; 61919-672; 61919-716; 63187-200; 63187-591; 68071-1760; 68071-2908; 68071-4548; 68788-8240; 70518-0895; 72789-224; 76420-192; 81964-225; 43063-820; 50090-0713; 50090-6056; 50090-6466; 53002-1369; 55289-019; 57237-028; 61919-401; 63187-044; 63187-295; 65862-071; 65862-706; 67296-1156; 68071-4455; 68788-7318; 68788-9948; 70518-2188; 70518-2190; 70518-3294; 71205-177; 71205-436; 76420-112; 76420-508; 0781-6039; 0093-4160; 0143-9285; 43063-341; 63187-262; 63629-7587; 63629-7798; 63629-7801; 68071-2766; 68071-2875; 68071-3119; 68788-6374; 68999-825; 55289-020; 63187-043; 63187-186; 63629-7633; 66267-994; 67296-1894; 68071-4693; 68071-4741; 68788-8324; 71205-035; 71205-422; 0781-6041; 16714-299; 0093-2267; 42571-234; 42708-153; 43063-574; 50090-0288; 50090-1512; 50090-1812; 50090-6351; 53002-2369; 63187-027; 67296-0986; 68071-2558; 68788-8209; 68788-8304; 68788-8325; 68788-9018; 71205-507; 76420-003; 52115-001; 65862-014; 65862-017; 50090-0406; 50090-0407; 50090-6469; 53002-2160; 57237-032; 63187-325; 68071-4953; 70518-2191; 70882-113; 70934-038; 76420-545; 16714-298; 0093-2264; 42708-010; 42708-076; 0143-9888; 0143-9939; 50090-1810; 53002-2090; 63187-029; 63187-399; 63187-880; 65862-707; 68071-2604; 70518-3234; 70882-114; 71205-266; 72789-254; 0781-2613; 0781-5061; 0781-6156; 42708-112; 43063-885; 50090-0301; 50090-0404; 50090-1086; 50090-1347; 61919-135; 63187-013; 63187-335; 63187-343; 63187-729; 65862-015; 65862-016; 65862-070; 68071-2320; 68071-2911; 70518-3228; 76420-573; 80425-0269; 0093-3109; 0093-4155; 50090-1513; 50090-1813; 50090-2251; 50090-6349; 57237-031; 61919-994; 63629-7585; 67296-1126; 68071-1826; 68788-6369; 68788-7323; 68788-8352; 68788-9019; 72189-463; 72789-225; 0781-6157; 81964-205; 83112-031; 0093-2263; 42571-233; 0143-9887; 50090-1826; 50090-6319; 50090-6355; 50436-0031; 53002-2091; 57237-033; 68071-3235; 68788-7414; 68788-9017; 68788-9949; 70934-064; 71205-775; 72189-285; 0781-2020; 76420-138; 82982-022; 0093-3107; 42708-078; 43063-915; 0143-9889; 50090-0302; 50090-0303; 50090-0405; 50090-0709; 50090-1811; 50090-6323; 57237-030; 59115-041
UNII 804826J2HU
Synonyms Amoxicillin | Amoxycillin | Amoxicilline | Amoxicillin Monopotassium Salt | Hydroxyampicillin | Amoxicillin Sodium | Amoxicillin Monosodium Salt | Amoxicillin, (R*)-Isomer | Amoxicillin Anhydrous | Actimoxi | BRL-2333 | BRL 2333 | BRL2333 | Clamoxyl | Penamox | Clamoxyl Parenteral | Clamoxyl G.A. | Polymox | Trimox | Wymox | Amoxicillin Trihydrate | Amoxil
Chemical Information
Molecular Formula C16H19N3O5S
CAS Registry Number 26787-78-0
SMILES CC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=C(C=C3)O)N)C(=O)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)
Abdominal discomfort07.01.06.001--Not Available
Abdominal pain07.01.05.0020.000257%
Abdominal pain upper07.01.05.0030.000222%
Abdominal rigidity07.01.05.0110.000005%Not Available
Abnormal faeces07.01.03.001--Not Available
Abortion spontaneous18.01.04.0010.000623%Not Available
Acne23.02.01.001--Not Available
Acute febrile neutrophilic dermatosis23.03.03.033; 01.02.01.0060.000022%Not Available
Acute hepatic failure09.01.03.0010.000034%Not Available
Acute psychosis19.03.01.0010.000010%Not Available
Acute respiratory distress syndrome24.03.02.034; 10.02.01.067; 22.01.03.0010.000017%
Affective disorder19.04.04.0010.000013%Not Available
Aggression19.05.01.0010.000043%Not Available
Agitation19.06.02.001; 17.02.05.012--
Agranulocytosis01.02.03.0010.000036%Not Available
Alanine aminotransferase increased13.03.04.005--
Alcohol intolerance14.02.01.001--
Anaemia01.03.02.001--
Anaphylactic reaction24.06.03.006; 10.01.07.0010.000543%
Anaphylactic shock24.06.02.004; 10.01.07.0020.000615%Not Available
Anaphylactoid reaction24.06.03.007; 10.01.07.0030.000024%Not Available
Angioedema10.01.05.009; 22.04.02.008; 23.04.01.0010.000625%Not Available
Anhedonia19.15.02.007--Not Available
Anosmia22.04.03.006; 17.04.04.0010.000005%
Anuria20.01.03.0020.000029%Not Available
Anxiety19.06.02.002--
Aphasia19.21.01.001; 17.02.03.001--
Aphthous ulcer07.05.06.0020.000026%Not Available
Aplastic anaemia01.03.03.0020.000005%Not Available
Arteriospasm coronary24.04.04.005; 02.02.02.005; 12.02.01.0310.000005%Not Available
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ADReCS-Target
Drug Name ADR Term Target
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