Adverse Drug Reaction Classification System

         

ADR Ontology
ADR Term Asthenia
ADR ID BADD_A00362
ADR Hierarchy
08      General disorders and administration site conditions
08.01      General system disorders NEC
08.01.01      Asthenic conditions
08.01.01.001      Asthenia
Description Clinical sign or symptom manifested as debility, or lack or loss of strength and energy. [MeSH]
MedDRA Code 10003549
MeSH ID D001247; D009440; D000073496
ADR Severity Grade (FAERS)
ADR Severity Grade (CTCAE) Not Available
Synonym
Adynamia | Asthenia | Collapse of legs | Debility | Debility marked | Debility, unspecified | Feeling of total lack of energy | Feelings of weakness | General debility | Loss of energy | Nervous debility | Neurasthaenia | Neurasthenia | Strength loss of | Weakness | Weakness generalised | Weakness generalized | Weakness postural | Energy decreased | Frailty | Weakness worsened | Hyposthenia | Cerebro-asthenic syndrome
Drugs Leading to the ADR
Drug IDDrug NameADR Frequency (FAERS)ADR Severity Grade (FAERS)
BADD_D01466Milnacipran hydrochloride--
BADD_D01469Miltefosine--
BADD_D01470Minocycline--
BADD_D01471Minocycline anion--
BADD_D01474Mipomersen sodium--
BADD_D01475Mirabegron--
BADD_D01476Mirtazapine--
BADD_D01477Misoprostol--
BADD_D01478Mitomycin--
BADD_D01479Mitotane0.000168%
BADD_D01480Mitoxantrone--
BADD_D01481Mitoxantrone hydrochloride--
BADD_D01483Moclobemide--
BADD_D01484Modafinil--
BADD_D01486Moexiprilat--
BADD_D01490Mometasone--
BADD_D01491Mometasone furoate--
BADD_D01496Montelukast--
BADD_D01497Montelukast sodium--
BADD_D01498Morphine--
BADD_D01499Morphine sulfate--
BADD_D01501Moxifloxacin--
BADD_D01502Moxifloxacin hydrochloride--
BADD_D01503Moxonidine--
BADD_D01506Muromonab-cd3--
BADD_D01507Mycophenolate mofetil--
BADD_D01508Mycophenolic acid--
BADD_D01510Nabilone--
BADD_D01511Nabumetone--
BADD_D01512Nadolol--
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ADReCS-Target
ADR Term Drug Name Target