MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Marasmus

(UMLS:C0086588)

UMLS ID:: C0086588
MeSH ID:: D011502

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.654.521.500.708.626

Synonym(s)

Marasmus

Athrepsia

Infantile atrophy

MARASMUS

Marantic atrophy

Marasmus infantilis

Marasmus lactantium

Marcor

Nutritional atrophy

10.

Nutritional marasmus

Associated Drug(s)

	Name	Number of Reports	Data Source
1	Rivastigmine	FAERS: 21	US FAERS
2	Leuprolide	FAERS: 15	US FAERS
3	Lenalidomide	FAERS: 11	US FAERS
4	Galantamine	FAERS: 8	US FAERS
5	Deferasirox	FAERS: 6	US FAERS
6	Valsartan	FAERS: 6	US FAERS
7	apixaban	FAERS: 6	US FAERS
8	Fentanyl	FAERS: 5	US FAERS
9	Zoledronic Acid	FAERS: 5	US FAERS
10	Ibandronic Acid	FAERS: 4	US FAERS
11	Telmisartan	FAERS: 4	US FAERS
12	Teriparatide	FAERS: 4	US FAERS
13	Bosentan	FAERS: 3	US FAERS
14	Dabigatran	FAERS: 3	US FAERS
15	Zonisamide	FAERS: 3	US FAERS
16	Atomoxetine Hydrochloride	FAERS: 2	US FAERS
17	Dasatinib	FAERS: 2	US FAERS
18	Edaravone	FAERS: 2	US FAERS
19	Eplerenone	FAERS: 2	US FAERS
20	Ferric Oxide, Saccharated	FAERS: 2	US FAERS
21	Lansoprazole	FAERS: 2	US FAERS
22	Memantine	FAERS: 2	US FAERS
23	Risperidone	FAERS: 2	US FAERS
24	Ruxolitinib phosphate	FAERS: 2	US FAERS
25	Sertraline	FAERS: 2	US FAERS
26	ambrisentan	FAERS: 2	US FAERS
27	bosutinib	FAERS: 2	US FAERS
28	Amiodarone	FAERS: 1	US FAERS
29	Ampicillin sodium mixture with sulbactam sodium	FAERS: 1	US FAERS
30	Bortezomib	FAERS: 1	US FAERS
31	Buprenorphine	FAERS: 1	US FAERS
32	Capecitabine	FAERS: 1	US FAERS
33	Cilostazol	FAERS: 1	US FAERS
34	Cyclosporine	FAERS: 1	OFFSIDES US FAERS
35	Diclofenac	FAERS: 1	US FAERS
36	Esomeprazole	FAERS: 1	US FAERS
37	Everolimus	FAERS: 1	US FAERS
38	Ferric citrate monohydrate	FAERS: 1	US FAERS
39	GS-7340	FAERS: 1	US FAERS
40	Hydroxyurea	FAERS: 1	US FAERS
41	Imatinib Mesylate	FAERS: 1	US FAERS
42	Imatinib Mesylate	FAERS: 1	US FAERS
43	Imipenem	FAERS: 1	US FAERS
44	Ivermectin	FAERS: 1	US FAERS
45	Linezolid	FAERS: 1	US FAERS
46	MDV 3100	FAERS: 1	US FAERS
47	Octreotide	FAERS: 1	US FAERS
48	Omacor	FAERS: 1	US FAERS
49	Pantoprazole	FAERS: 1	US FAERS
50	QVA149	FAERS: 1	US FAERS
51	Sildenafil Citrate	FAERS: 1	US FAERS
52	Sitagliptin Phosphate	FAERS: 1	US FAERS
53	Tadalafil	FAERS: 1	US FAERS
54	Telbivudine	FAERS: 1	US FAERS
55	Tenofovir	FAERS: 1	US FAERS
56	Valproic Acid	FAERS: 1	US FAERS
57	Venlafaxine Hydrochloride	FAERS: 1	US FAERS
58	acetyl-2-naphthylalanyl-3-chlorophenylalanyl-1-oxohexadecyl-seryl-4-aminophenylalanyl(hydroorotyl)-4-aminophenylalanyl(carbamoyl)-leucyl-ILys-prolyl-alaninamide	FAERS: 1	US FAERS
59	carbidopa, levodopa drug combination	FAERS: 1	US FAERS
60	edoxaban	FAERS: 1	US FAERS
61	eltrombopag	FAERS: 1	US FAERS
62	empagliflozin	FAERS: 1	US FAERS
63	pomalidomide	FAERS: 1	US FAERS
64	regorafenib	FAERS: 1	US FAERS
65	repaglinide	FAERS: 1	US FAERS
66	Disulfiram		OFFSIDES
67	Estrogens, Conjugated (USP)		OFFSIDES
68	Etodolac		OFFSIDES
69	Fluvoxamine		OFFSIDES
70	Fosinopril		OFFSIDES
71	Ivermectin		OFFSIDES
72	Ketoconazole		OFFSIDES
73	Mycophenolic Acid		OFFSIDES
74	Penicillin V		OFFSIDES
75	Solifenacin Succinate		OFFSIDES
76	Thymidine		OFFSIDES
77	Trichlormethiazide		OFFSIDES
78	adefovir dipivoxil		OFFSIDES
79	azelnidipine		OFFSIDES
80	bicalutamide		OFFSIDES
81	crotamiton		OFFSIDES
82	hydrocodone tartrate, ibuprofen drug combination		OFFSIDES
83	isosorbide-5-mononitrate		OFFSIDES
84	moxonidine		OFFSIDES
85	pantethine		OFFSIDES
86	pyranoprofen		OFFSIDES
87	urapidil		OFFSIDES
88	valdecoxib		OFFSIDES

Similar ADE(s)

	Name	Semantic Similarity
1	Magnesium Deficiency	36%
2	Potassium Deficiency	36%
3	Avitaminosis	36%
4	Starvation	28.5%
5	Refeeding Syndrome	28.5%
6	Ascorbic Acid Deficiency	23.8%
7	Vitamin A Deficiency	23.8%
8	Vitamin D Deficiency	23.8%
9	Vitamin E Deficiency	23.8%
10	Child Nutrition Disorders	22.7%
11	Hypervitaminosis A	22.7%
12	Infant Nutrition Disorders	22.7%
13	Wasting Syndrome	20.6%
14	Folic Acid Deficiency	17.8%
15	Pellagra	17.8%
16	Thiamine Deficiency	17.8%
17	Vitamin B 12 Deficiency	17.8%
18	Vitamin B 6 Deficiency	17.8%
19	Pyridoxine Deficiency	17.8%
20	Kwashiorkor	16.8%
21	Metabolic Diseases	15.3%
22	Beriberi	14.8%
23	Vitamin K Deficiency	12.2%
24	Rickets	10.6%
25	Anemia, Pernicious	9.9%
26	Hyperhomocysteinemia	9.8%
27	Scurvy	9.1%
28	Osteomalacia	7.9%
29	Acid-Base Imbalance	7.6%
30	Calcium Metabolism Disorders	7.6%
31	Iron Metabolism Disorders	7.6%
32	Phosphorus Metabolism Disorders	7.6%
33	Water-Electrolyte Imbalance	7.6%
34	Lipid Metabolism Disorders	7.6%
35	Mitochondrial Diseases	7.6%
36	Glucose Metabolism Disorders	7.6%
37	Wernicke Encephalopathy	6.4%
38	Hypercalcemia	5.5%
39	Hypocalcemia	5.5%
40	Milk-Alkali Syndrome	5.5%
41	HIV Wasting Syndrome	5.4%
42	Subacute Combined Degeneration	5.2%
43	Osteopenia	5.1%
44	Brain Diseases, Metabolic	5%
45	Renal Osteodystrophy	5%
46	Renal rickets	5%
47	Obesity	4.8%
48	Lipodystrophy	4.1%
49	Acidosis	4.1%
50	Alkalosis	4.1%
51	Amyloidosis	4.1%
52	Calcinosis	4.1%
53	Hyperglycemia	4.1%
54	Hyperinsulinism	4.1%
55	Hyperkalemia	4.1%
56	Hypernatremia	4.1%
57	Hypoglycemia	4.1%
58	Hypokalemia	4.1%
59	Hyponatremia	4.1%
60	Xanthomatosis	4.1%
61	Hypophosphatemia	4.1%
62	Metabolic acidosis	4.1%
63	Dyslipidemias	4.1%
64	Iron Overload	4.1%
65	Xanthoma	4.1%
66	Obesity, Abdominal	3.6%
67	Pseudohypoparathyroidism	3.5%
68	Familial Hypophosphatemic Rickets	3.5%
69	Brain Diseases, Metabolic, Inborn	3.3%
70	Diabetes Mellitus	2.9%
71	Pediatric Obesity	2.9%
72	Dehydration	2.8%
73	Lipomatosis	2.8%
74	Water Intoxication	2.8%
75	Werner Syndrome	2.8%
76	Achlorhydria	2.7%
77	Amino Acid Metabolism, Inborn Errors	2.7%
78	Bloom Syndrome	2.7%
79	Carbohydrate Metabolism, Inborn Errors	2.7%
80	Metal Metabolism, Inborn Errors	2.7%
81	Osteoporosis	2.7%
82	Progeria	2.7%
83	Lysosomal Storage Diseases	2.7%
84	Bone Demineralization, Pathologic	2.7%
85	Cytochrome-c Oxidase Deficiency	2.7%
86	Peroxisomal Disorders	2.7%
87	Post-Traumatic Osteoporosis	2.7%
88	Celiac Disease	2.7%
89	Sprue, Tropical	2.7%
90	Steatorrhea	2.7%
91	Sprue	2.7%
92	Leigh Disease	2.6%
93	Lactose Intolerance	2.6%
94	Prader-Willi Syndrome	2.5%
95	Hypolipoproteinemias	2.4%
96	Acidosis, Lactic	2.4%
97	Calciphylaxis	2.4%
98	Hemosiderosis	2.4%
99	Ketosis	2.4%
100	Ketonuria	2.4%
101	Ketoacidosis	2.4%
102	Ketonemia	2.4%
103	Vascular calcification	2.4%
104	Carbamoyl-Phosphate Synthase I Deficiency Disease	2.2%
105	Mitochondrial Encephalomyopathies	2.2%
106	Mitochondrial Myopathies	2.1%
107	Smith-Lemli-Opitz Syndrome	2.1%
108	Myelinolysis, Central Pontine	2.1%
109	Galactosemias	2.1%
110	Urea Cycle Disorders, Inborn	2.1%
111	Tyrosinemias	2.1%
112	Glycosuria	2%
113	Reye Syndrome	2%
114	Hepatic Encephalopathy	2%
115	Diabetic Ketoacidosis	2%
116	Congenital Hyperinsulinism	2%
117	Hyperlipidemia, Familial Combined	2%
118	Hyperlipoproteinemia Type IV	1.9%
119	Hyperlipoproteinemia Type V	1.9%
120	Hyperphosphaturia	1.8%
121	Hyperlipoproteinemia Type III	1.8%
122	Porphyrias, Hepatic	1.7%
123	Necrobiosis Lipoidica Diabeticorum	1.6%
124	Acidosis, Respiratory	1.6%
125	Adiposis Dolorosa	1.6%
126	Alkalosis, Respiratory	1.6%
127	Homocystinuria	1.6%
128	Fanconi Anemia	1.6%
129	Renal tubular acidosis	1.6%
130	Alkaptonuria	1.6%
131	Glycogen Storage Disease	1.6%
132	Hypophosphatasia	1.6%
133	Insulin Resistance	1.6%
134	Osteoporosis, Postmenopausal	1.6%
135	Propionic acidemia	1.6%
136	Dihydropyrimidine Dehydrogenase Deficiency	1.6%
137	Cystinosis	1.6%
138	Hypercholesterolemia	1.6%
139	Hyperlipoproteinemias	1.6%
140	Hypertriglyceridemia	1.6%
141	Hypoalphalipoproteinemias	1.6%
142	Amyloid Neuropathies, Familial	1.4%
143	Glycogen storage disease type II	1.4%
144	HIV-Associated Lipodystrophy Syndrome	1.4%
145	Neuronal Ceroid-Lipofuscinoses	1.3%
146	Friedreich Ataxia	1.3%
147	Zellweger Syndrome	1.3%
148	Menkes Kinky Hair Syndrome	1.3%
149	Nesidioblastosis	1.3%
150	MELAS Syndrome	1.3%
151	Gestational Diabetes	1.3%
152	Latent Autoimmune Diabetes in Adults	1.3%
153	Gaucher Disease	1.3%
154	Diabetes Mellitus, Experimental	1.2%
155	Adrenoleukodystrophy	1.2%
156	Hepatolenticular Degeneration	1.2%
157	Nephrocalcinosis	1.2%
158	Tetany	1.2%
159	Refsum Disease	1.2%
160	Glycosuria, Renal	1.2%
161	Cerebral Amyloid Angiopathy	1.2%
162	Kernicterus	1.2%
163	Cockayne Syndrome	1.2%
164	Mucopolysaccharidosis III	1.1%
165	Glycogen Storage Disease Type I	1.1%
166	Glycogen Storage Disease Type V	1.1%
167	Ataxia Telangiectasia	1%
168	Kearns-Sayre syndrome	1%
169	Optic Atrophy, Hereditary, Leber	1%
170	Familial Periodic Paralysis	1%
171	Primary amyloidosis	1%
172	Fabry Disease	1%
173	Variegate Porphyria	1%
174	Acute intermittent porphyria	1%
175	Porphyria Cutanea Tarda	1%
176	Renal Aminoacidurias	1%
177	Fanconi Syndrome	1%
178	Pseudohypoaldosteronism	1%
179	Liddle Syndrome	1%
180	Niemann-Pick Disease, Type C	0.9%
181	Xeroderma Pigmentosum	0.9%
182	Tay-Sachs Disease	0.9%
183	Gout	0.8%
184	Amyotrophic Lateral Sclerosis	0.8%
185	Sjogren-Larsson Syndrome	0.8%
186	Antley-Bixler Syndrome Phenotype	0.8%
187	Canavan Disease	0.7%
188	Alexander Disease	0.7%
189	Mucopolysaccharidosis II	0.7%
190	CREST Syndrome	0.7%
191	Hypokalemic periodic paralysis	0.6%
192	Frontotemporal dementia	0.6%
193	Cystinuria	0.6%
194	Albinism	0.6%
195	Arthritis, Gouty	0.5%
196	Ichthyosis, X-Linked	0.5%

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