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2022 Update-Veterinary Drugs & Uses
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DrugCentral 2023 🐕
2022 Update-Veterinary Drugs & Uses
Search
Structure 🔎
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L1000
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All
FDA-approved
EMA-approved
PMDA-approved
Target Card Uniprot Example:
P23975
phosphoric acid 🐶
Veterinary Use |
Indications/Contra
| FAERs-F
| FAERs-M
| Orange Bk
| BioActivity |
Stem definition
Drug id
CAS RN
4478
7664-38-2
Description:
Molecule
Description
Molfile
Inchi
Smiles
Synonyms:
phosphoric acid
concise etchant is 37% H3PO4
Molecular weight: 97.99
Formula: H3O4P
CLOGP: -2.17
LIPINSKI: None
HAC: 4
HDO: 3
TPSA: 77.76
ALOGS:
ROTB: 0
Drug dosage:
None
ADMET properties:
None
Approvals:
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Date
Agency
Company
Orphan
Sept. 24, 1971
FDA
B BRAUN
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FDA Adverse Event Reporting System (Female)
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MedDRA adverse event term
Likelihood ratio
Likelihood ratio threshold
Patients taking drug having adverse event
Patients taking drug not having adverse event
Patients not taking drug having adverse event
Patients not taking drug not having adverse event
Skin candida
115.92
19.61
27
5218
1628
63482149
Creatinine renal clearance decreased
114.42
19.61
45
5200
16263
63467514
Sedation complication
107.11
19.61
41
5204
13781
63469996
Balance disorder
103.46
19.61
72
5173
84350
63399427
Blood calcium decreased
102.68
19.61
48
5197
26403
63457374
Orthostatic hypotension
96.92
19.61
51
5194
36109
63447668
Constipation
80.80
19.61
96
5149
224847
63258930
Cognitive disorder
76.39
19.61
51
5194
55764
63428013
Sedation
71.99
19.61
43
5202
38766
63445011
Depressed level of consciousness
71.48
19.61
51
5194
62027
63421750
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FDA Adverse Event Reporting System (Male)
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MedDRA adverse event term
Likelihood ratio
Likelihood ratio threshold
Patients taking drug having adverse event
Patients taking drug not having adverse event
Patients not taking drug having adverse event
Patients not taking drug not having adverse event
Periarthritis
30.37
21.26
8
2144
1076
34953703
Dehydration
27.86
21.26
37
2115
129932
34824847
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FDA Adverse Event Reporting System (Geriatric)
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MedDRA adverse event term
Likelihood ratio
Likelihood ratio threshold
Patients taking drug having adverse event
Patients taking drug not having adverse event
Patients not taking drug having adverse event
Patients not taking drug not having adverse event
Creatinine renal clearance decreased
134.30
17.68
51
5786
18951
79719600
Sedation complication
125.13
17.68
46
5791
15623
79722928
Blood calcium decreased
121.47
17.68
55
5782
31764
79706787
Balance disorder
117.52
17.68
79
5758
98778
79639773
Skin candida
107.77
17.68
26
5811
2061
79736490
Orthostatic hypotension
94.60
17.68
56
5781
56108
79682443
Cognitive disorder
85.73
17.68
57
5780
69869
79668682
Constipation
80.27
17.68
101
5736
282949
79455602
Sedation
75.19
17.68
47
5790
51848
79686703
Depressed level of consciousness
58.97
17.68
52
5785
96600
79641951
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FDA Adverse Event Reporting System (Pediatric)
None
Pharmacologic Action:
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Source
Code
Description
CHEBI has role
CHEBI:33287
fertilizers
CHEBI has role
CHEBI:46787
solvents
CHEBI has role
CHEBI:77746
Homo sapiens metabolite
CHEBI has role
CHEBI:84735
algal metabolites
MeSH PA
D003764
Dental Materials
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Drug Use
| Suggest Off label Use Form|
|View source of the data|
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Disease
Relation
SNOMED_ID
DOID
Nutritional support
indication
278906000
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🐶 Veterinary Drug Use
None
🐶 Veterinary products
None
Acid dissociation constants calculated using MoKa v3.0.0
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Dissociation level
Dissociation constant
Type (acidic/basic)
pKa1
1.0
acidic
pKa2
6.06
acidic
pKa3
11.11
acidic
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Orange Book patent data (new drug applications)
None
Orange Book exclusivity data (new drug applications)
None
Bioactivity Summary:
None
External reference:
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ID
Source
006128
NDDF
1004
PUBCHEM_CID
2HP
PDB_CHEM_ID
4018718
VUID
4018718
VANDF
8259
RXNORM
C0031700
UMLSCUI
C030242
MESH_SUPPLEMENTAL_RECORD_UI
CHEBI:26078
CHEBI
CHEMBL1187
ChEMBL_ID
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Pharmaceutical products:
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Product
Category
Ingredients
NDC
Form
Quantity
Route
Marketing
Label
Anti Nausea
HUMAN OTC DRUG LABEL
3
0536-1302
LIQUID
21.50 mg
ORAL
Unapproved drug other
13 sections
Anti Nausea
HUMAN OTC DRUG LABEL
3
0536-1302
LIQUID
21.50 mg
ORAL
Unapproved drug other
13 sections
Anti Nausea Liquid
HUMAN OTC DRUG LABEL
3
36800-708
SOLUTION
21.50 mg
ORAL
Unapproved drug other
13 sections
Anti Nausea Liquid
HUMAN OTC DRUG LABEL
3
36800-708
SOLUTION
21.50 mg
ORAL
Unapproved drug other
13 sections
equaline anti nausea
HUMAN OTC DRUG LABEL
3
41163-630
SOLUTION
21.50 mg
ORAL
Unapproved drug other
14 sections
formula em
HUMAN OTC DRUG LABEL
3
0904-0049
SOLUTION
21.50 mg
ORAL
Unapproved drug other
14 sections
FreAmine III
HUMAN PRESCRIPTION DRUG LABEL
16
0264-9010
INJECTION, SOLUTION
0.12 g
INTRAVENOUS
NDA
24 sections
FreAmine III
HUMAN PRESCRIPTION DRUG LABEL
16
0264-9011
INJECTION, SOLUTION
0.12 g
INTRAVENOUS
NDA
24 sections
Good Neighbor Anti NauseaCherry Flavor
HUMAN OTC DRUG LABEL
3
46122-729
LIQUID
21.50 mg
ORAL
Unapproved drug other
13 sections
Good Neighbor Anti NauseaCherry Flavor
HUMAN OTC DRUG LABEL
3
46122-729
LIQUID
21.50 mg
ORAL
Unapproved drug other
13 sections
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Structure 🔎
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L1000
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phosphoric acid