MetaADEDB 2.0 @ LMMD
Imodium Multi-Symptom Relief
(RBAIODSXIDHVCD-UHFFFAOYSA-N)
Structure
SMILES
Clc1ccc(cc1)C1(O)CCN(CC1)CCC(C(=O)N(C)C)(c1ccccc1)c1ccccc1.CO[Si](O[Si](C)(C)C)(C)C.O=[Si]=O.Cl
Molecular Formula:
C35H52Cl2N2O6Si3
Molecular Weight:
751.960
Log P:
7.3956
Hydrogen Bond Acceptor:
8
Hydrogen Bond Donor:
2
TPSA:
96.38
CAS Number(s):
137524-29-9
Synonym(s)
1.
Imodium Multi-Symptom Relief
External Link(s)
PubChem Compound91826217
Adverse Drug Event(s)
NameNumber of ReportsReference(s)Data Source
1Drug ineffectiveFAERS: 721US FAERS
2Incorrect dose administeredFAERS: 399US FAERS
3Product size issueFAERS: 259US FAERS
4Inappropriate schedule of drug administrationFAERS: 210US FAERS
5Product use issueFAERS: 188US FAERS
6Product packaging issueFAERS: 177US FAERS
7Expired product administeredFAERS: 169US FAERS
8Wrong technique in drug usage processFAERS: 165US FAERS
9ChokingFAERS: 151US FAERS
10Product difficult to swallowFAERS: 140US FAERS
11Wrong technique in product usage processFAERS: 133US FAERS
12Intentional product use issueFAERS: 125US FAERS
13Product use complaintFAERS: 110US FAERS
14Product quality issueFAERS: 103US FAERS
15RetchingFAERS: 93US FAERS
16Product label issueFAERS: 91US FAERS
17ConstipationFAERS: 79US FAERS
18Intentional product misuseFAERS: 79US FAERS
19OverdoseFAERS: 73US FAERS
20Product physical issueFAERS: 68US FAERS
21Product coating issueFAERS: 67US FAERS
22Drug prescribing errorFAERS: 50US FAERS
23Drug administration errorFAERS: 46US FAERS
24Therapeutic response unexpectedFAERS: 43US FAERS
25DysgeusiaFAERS: 40US FAERS
26NauseaFAERS: 34US FAERS
27VomitingFAERS: 34US FAERS
28FlatulenceFAERS: 32US FAERS
29Product blister packaging issueFAERS: 29US FAERS
30Product solubility abnormalFAERS: 28US FAERS
31MalaiseFAERS: 27US FAERS
32Product taste abnormalFAERS: 27US FAERS
33Product package associated injuryFAERS: 26US FAERS
34DizzinessFAERS: 24US FAERS
35Foreign body in respiratory tractFAERS: 24US FAERS
36Product formulation issueFAERS: 24US FAERS
37Product use in unapproved indicationFAERS: 24US FAERS
38Product lot number issueFAERS: 23US FAERS
39Infrequent bowel movementsFAERS: 21US FAERS
40Choking sensationFAERS: 18US FAERS
41Inappropriate schedule of product administrationFAERS: 18US FAERS
42Incorrect drug administration durationFAERS: 18US FAERS
43Therapeutic response delayedFAERS: 18US FAERS
44FatigueFAERS: 16US FAERS
45SomnolenceFAERS: 15US FAERS
46Drug ineffective for unapproved indicationFAERS: 14US FAERS
47Abdominal discomfortFAERS: 13US FAERS
48Accidental exposure to productFAERS: 12US FAERS
49Throat irritationFAERS: 12US FAERS
50Adverse eventFAERS: 11US FAERS
51Oropharyngeal painFAERS: 11US FAERS
52Medication ErrorFAERS: 10US FAERS
53Product administration errorFAERS: 10US FAERS
54Product label confusionFAERS: 10US FAERS
55Product expiration date issueFAERS: 8US FAERS
56Product packaging quantity issueFAERS: 8US FAERS
57Abdominal PainFAERS: 6US FAERS
58OnychoclasisFAERS: 6US FAERS
59PainFAERS: 6US FAERS
60Product shape issueFAERS: 6US FAERS
61PruritusFAERS: 6US FAERS
62UrticariaFAERS: 6US FAERS
63DiscomfortFAERS: 5US FAERS
64HeadacheFAERS: 5US FAERS
65Product closure removal difficultFAERS: 5US FAERS
66AphagiaFAERS: 4US FAERS
67AstheniaFAERS: 4US FAERS
68Chest PainFAERS: 4US FAERS
69DyspepsiaFAERS: 4US FAERS
70HypersensitivityFAERS: 4US FAERS
71Incorrect product administration durationFAERS: 4US FAERS
72Incorrect route of drug administrationFAERS: 4US FAERS
73LacerationFAERS: 4US FAERS
74Physical product label issueFAERS: 4US FAERS
75Product availability issueFAERS: 4US FAERS
76Product complaintFAERS: 4US FAERS
77Product container seal issueFAERS: 4US FAERS
78Product friableFAERS: 4US FAERS
79Drug dose omissionFAERS: 3US FAERS
80Drug effect incompleteFAERS: 3US FAERS
81DysphoniaFAERS: 3US FAERS
82DysuriaFAERS: 3US FAERS
83Feeling abnormalFAERS: 3US FAERS
84Irritable Bowel SyndromeFAERS: 3US FAERS
85Peripheral swellingFAERS: 3US FAERS
86Product container issueFAERS: 3US FAERS
87Product outer packaging issueFAERS: 3US FAERS
88Product physical consistency issueFAERS: 3US FAERS
89Product selection errorFAERS: 3US FAERS
90TremorFAERS: 3US FAERS
91Visual ImpairmentFAERS: 3US FAERS
92Accidental exposure to product by childFAERS: 2US FAERS
93Accidental overdoseFAERS: 2US FAERS
94Blood glucose increasedFAERS: 2US FAERS
95ChromaturiaFAERS: 2US FAERS
96DehydrationFAERS: 2US FAERS
97DisabilityFAERS: 2US FAERS
98Drug effect delayedFAERS: 2US FAERS
99EructationFAERS: 2US FAERS
100Expired drug administeredFAERS: 2US FAERS
101GastritisFAERS: 2US FAERS
102Gastrointestinal sounds abnormalFAERS: 2US FAERS
103GoutFAERS: 2US FAERS
104HungerFAERS: 2US FAERS
105HypersomniaFAERS: 2US FAERS
106Limb injuryFAERS: 2US FAERS
107Medication residue presentFAERS: 2US FAERS
108Opiates positiveFAERS: 2US FAERS
109Pharmaceutical product counterfeitFAERS: 2US FAERS
110Prescribed overdoseFAERS: 2US FAERS
111Product comminglingFAERS: 2US FAERS
112Product packaging difficult to openFAERS: 2US FAERS
113Product prescribing errorFAERS: 2US FAERS
114Reaction to drug excipientsFAERS: 2US FAERS
115Rectal dischargeFAERS: 2US FAERS
116Suspected counterfeit productFAERS: 2US FAERS
117Therapy changeFAERS: 2US FAERS
118Unevaluable eventFAERS: 2US FAERS
119Unintentional use for unapproved indicationFAERS: 2US FAERS
120Amphetamines positiveFAERS: 1US FAERS
121ArthralgiaFAERS: 1US FAERS
122Blood magnesium decreasedFAERS: 1US FAERS
123Blood potassium decreasedFAERS: 1US FAERS
124Blood potassium increasedFAERS: 1US FAERS
125CholelithiasisFAERS: 1US FAERS
126Clostridium difficile colitisFAERS: 1US FAERS
127DependenceFAERS: 1US FAERS
128Drug DependenceFAERS: 1US FAERS
129Drug abuseFAERS: 1US FAERS
130Drug dispensing errorFAERS: 1US FAERS
131Drug diversionFAERS: 1US FAERS
132Drug screen false positiveFAERS: 1US FAERS
133ErythemaFAERS: 1US FAERS
134Exposure during breast feedingFAERS: 1US FAERS
135Eye irritationFAERS: 1US FAERS
136Eye painFAERS: 1US FAERS
137Feeling ColdFAERS: 1US FAERS
138FlushingFAERS: 1US FAERS
139Gastrointestinal hypomotilityFAERS: 1US FAERS
140Gingival erythemaFAERS: 1US FAERS
141HepatitisFAERS: 1US FAERS
142Impaired work abilityFAERS: 1US FAERS
143Incorrect product formulation administeredFAERS: 1US FAERS
144Incorrect product storageFAERS: 1US FAERS
145InfluenzaFAERS: 1US FAERS
146Intercepted medication errorFAERS: 1US FAERS
147Maternal exposure during pregnancyFAERS: 1US FAERS
148Memory impairmentFAERS: 1US FAERS
149Musculoskeletal chest painFAERS: 1US FAERS
150MyalgiaFAERS: 1US FAERS
151Myocardial InfarctionFAERS: 1US FAERS
152Neck PainFAERS: 1US FAERS
153PalpitationsFAERS: 1US FAERS
154PancreatitisFAERS: 1US FAERS
155Poor quality drug administeredFAERS: 1US FAERS
156PregnancyFAERS: 1US FAERS
157PresyncopeFAERS: 1US FAERS
158Product dose omissionFAERS: 1US FAERS
159Product storage errorFAERS: 1US FAERS
160Product used for unknown indicationFAERS: 1US FAERS
161Pulmonary painFAERS: 1US FAERS
162Rash erythematousFAERS: 1US FAERS
163Rectal tenesmusFAERS: 1US FAERS
164RegurgitationFAERS: 1US FAERS
165SepsisFAERS: 1US FAERS
166Slow speechFAERS: 1US FAERS
167SluggishnessFAERS: 1US FAERS
168SwellingFAERS: 1US FAERS
169Tablet physical issueFAERS: 1US FAERS
170Therapeutic reaction time decreasedFAERS: 1US FAERS
171ThirstFAERS: 1US FAERS
172Toxicity to various agentsFAERS: 1US FAERS
173Urinary hesitationFAERS: 1US FAERS
174Vaginal DischargeFAERS: 1US FAERS
175VertigoFAERS: 1US FAERS
176Wrong product administeredFAERS: 1US FAERS
177prostatitisFAERS: 1US FAERS
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