megestrol acetate ๐Ÿถ Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | BioActivity |

Stem definitionDrug idCAS RN
steroids, progestogens 1667 595-33-5

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • megestrol acetate
  • magestin
  • megestryl acetate
  • niagestin
Megestrol acetate is a progestogen with actions and uses similar to those of the progestogens in general. It also has anti-androgenic properties. It is given by mouth in the palliative treatment or as an adjunct to other therapy in endometrial carcinoma and in breast cancer. Megestrol acetate has been approved to treat anorexia and cachexia. (From Reynolds JEF(Ed): Martindale: The Extra Pharmacopoeia (electronic version). Micromedex, Inc, Englewood, CO, 1995)
  • Molecular weight: 384.52
  • Formula: C24H32O4
  • CLOGP: 3.77
  • LIPINSKI: 0
  • HAC: 4
  • HDO: 0
  • TPSA: 60.44
  • ALOGS: -5.06
  • ROTB: 3

  • Status: OFP

  • Legend:
    OFP - off patent
    OFM - off market
    ONP - on patent

Drug dosage:

DoseUnitRoute
5 mg O
0.16 g O

ADMET properties:

PropertyValueReference
BDDCS (Biopharmaceutical Drug Disposition Classification System) 2 Bocci G, Oprea TI, Benet LZ
S (Water solubility) 0.00 mg/mL Benet LZ, Broccatelli F, Oprea TI
EoM (Fraction excreted unchanged in urine) 60 % Benet LZ, Broccatelli F, Oprea TI
MRTD (Maximum Recommended Therapeutic Daily Dose) 23.22 ยตM/kg/day Contrera JF, Matthews EJ, Kruhlak NL, Benz RD
BA (Bioavailability) 90 % Kim MT, Sedykh A, Chakravarti SK, Saiakhov RD, Zhu H

Approvals:

DateAgencyCompanyOrphan
Aug. 18, 1971 FDA BRISTOL MYERS SQUIBB

FDA Adverse Event Reporting System (Female)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Death 116.32 20.43 154 5499 374227 63109142
Decreased appetite 98.14 20.43 116 5537 250936 63232433
Malignant neoplasm progression 71.74 20.43 59 5594 82062 63401307
Neutropenia 68.48 20.43 81 5572 174924 63308445
Disease progression 56.77 20.43 62 5591 122696 63360673
Deep vein thrombosis 56.60 20.43 52 5601 83748 63399621
Metastases to liver 51.88 20.43 30 5623 23609 63459760
Dehydration 48.52 20.43 68 5585 173286 63310083
Asthenia 41.97 20.43 100 5553 383504 63099865
Diarrhoea 38.57 20.43 145 5508 715221 62768148
Metastases to bone 36.61 20.43 23 5630 20996 63462373
Hypoaesthesia oral 29.82 20.43 17 5636 13016 63470353
Abdominal pain 28.33 20.43 73 5580 293383 63189986
Oestrogen receptor assay positive 28.29 20.43 7 5646 505 63482864
Meningioma 27.41 20.43 11 5642 3874 63479495
Papillary thyroid cancer 25.43 20.43 9 5644 2247 63481122
Gastritis 24.86 20.43 23 5630 37280 63446089
Dysgeusia 24.04 20.43 25 5628 46685 63436684
Neutropenic sepsis 23.75 20.43 16 5637 16422 63466947
Breast cancer 23.31 20.43 25 5628 48358 63435011
Thoracic vertebral fracture 22.39 20.43 10 5643 4582 63478787
Anaemia 22.37 20.43 67 5586 293363 63190006
Nausea 21.83 20.43 140 5513 854331 62629038
Pulmonary embolism 21.74 20.43 38 5615 116646 63366723
Constipation 21.72 20.43 56 5597 224887 63258482

FDA Adverse Event Reporting System (Male)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Malignant neoplasm progression 77.72 18.63 88 6327 87958 34862558
Death 76.80 18.63 201 6214 397848 34552668
Respiratory tract infection bacterial 75.19 18.63 23 6392 1759 34948757
Respiratory tract infection viral 71.32 18.63 24 6391 2493 34948023
Asthenia 68.08 18.63 143 6272 245108 34705408
Decreased appetite 65.93 18.63 113 6302 166279 34784237
Dehydration 63.35 18.63 97 6318 129872 34820644
Adrenal insufficiency 58.95 18.63 35 6380 14012 34936504
Pneumonia 54.94 18.63 168 6247 362459 34588057
Pulmonary embolism 52.41 18.63 73 6342 89673 34860843
Fatigue 44.68 18.63 159 6256 370494 34580022
Disease progression 38.31 18.63 70 6345 108007 34842509
Anaemia 35.07 18.63 108 6307 233227 34717289
Respiratory tract infection 32.97 18.63 28 6387 19684 34930832
Plasma cell myeloma 30.38 18.63 38 6377 41999 34908517
Diarrhoea 28.68 18.63 144 6271 389768 34560748
Drug ineffective 26.49 18.63 27 6388 456724 34493792
Weight decreased 23.16 18.63 78 6337 176223 34774293
Dysphagia 22.82 18.63 41 6374 62340 34888176
Platelet count decreased 21.36 18.63 59 6356 119658 34830858
Thrombocytopenia 21.29 18.63 70 6345 156177 34794339
Androgen deficiency 19.42 18.63 5 6410 203 34950313

FDA Adverse Event Reporting System (Geriatric)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Death 130.76 17.59 231 8794 566283 79169080
Decreased appetite 110.77 17.59 163 8862 342255 79393108
Dehydration 97.85 17.59 130 8895 248057 79487306
Respiratory tract infection bacterial 82.68 17.59 23 9002 2054 79733309
Adrenal insufficiency 74.31 17.59 44 8981 28443 79706920
Malignant neoplasm progression 74.21 17.59 84 8941 135906 79599457
Pulmonary embolism 73.94 17.59 94 8931 171560 79563803
Asthenia 71.69 17.59 170 8855 511519 79223844
Respiratory tract infection viral 70.30 17.59 24 9001 4235 79731128
Pneumonia 69.54 17.59 197 8828 660049 79075314
Disease progression 54.08 17.59 84 8941 184278 79551085
Plasma cell myeloma 49.57 17.59 44 8981 53215 79682148
Anaemia 48.87 17.59 135 8890 444880 79290483
Neutropenia 46.15 17.59 101 8924 287609 79447754
Diarrhoea 44.63 17.59 207 8818 880282 78855081
Platelet count decreased 34.25 17.59 71 8954 194593 79540770
Deep vein thrombosis 33.90 17.59 54 8971 120865 79614498
Drug ineffective 33.68 17.59 44 8981 1080869 78654494
Fatigue 32.24 17.59 197 8828 929530 78805833
Thrombocytopenia 28.57 17.59 80 8945 265179 79470184
Respiratory tract infection 28.10 17.59 31 8994 48658 79686705
Constipation 26.31 17.59 81 8944 282969 79452394
Mental status changes 26.17 17.59 35 8990 66924 79668439
Pleural effusion 25.56 17.59 53 8972 145209 79590154
Androgen deficiency 25.13 17.59 5 9020 102 79735261
Failure to thrive 25.03 17.59 16 9009 11828 79723535
Meningioma 23.80 17.59 11 9014 4287 79731076
Blood testosterone decreased 22.87 17.59 9 9016 2368 79732995
Secondary adrenocortical insufficiency 20.80 17.59 9 9016 3005 79732358
Hypoaesthesia oral 20.19 17.59 15 9010 14109 79721254
Malnutrition 19.76 17.59 18 9007 22484 79712879
Hypophagia 19.73 17.59 25 9000 45342 79690021
Cachexia 18.66 17.59 13 9012 11070 79724293
Dysphagia 18.54 17.59 42 8983 122094 79613269
Lethargy 18.38 17.59 33 8992 81259 79654104
Dysgeusia 18.06 17.59 27 8998 57150 79678213
Sepsis 17.92 17.59 69 8956 269359 79466004
Toxicity to various agents 17.87 17.59 13 9012 421527 79313836

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
ATC G03AA04 GENITO URINARY SYSTEM AND SEX HORMONES
SEX HORMONES AND MODULATORS OF THE GENITAL SYSTEM
HORMONAL CONTRACEPTIVES FOR SYSTEMIC USE
Progestogens and estrogens, fixed combinations
ATC G03AB01 GENITO URINARY SYSTEM AND SEX HORMONES
SEX HORMONES AND MODULATORS OF THE GENITAL SYSTEM
HORMONAL CONTRACEPTIVES FOR SYSTEMIC USE
Progestogens and estrogens, sequential preparations
ATC G03AC05 GENITO URINARY SYSTEM AND SEX HORMONES
SEX HORMONES AND MODULATORS OF THE GENITAL SYSTEM
HORMONAL CONTRACEPTIVES FOR SYSTEMIC USE
Progestogens
ATC G03DB02 GENITO URINARY SYSTEM AND SEX HORMONES
SEX HORMONES AND MODULATORS OF THE GENITAL SYSTEM
PROGESTOGENS
Pregnadien derivatives
ATC G03FA08 GENITO URINARY SYSTEM AND SEX HORMONES
SEX HORMONES AND MODULATORS OF THE GENITAL SYSTEM
PROGESTOGENS AND ESTROGENS IN COMBINATION
Progestogens and estrogens, fixed combinations
ATC G03FB04 GENITO URINARY SYSTEM AND SEX HORMONES
SEX HORMONES AND MODULATORS OF THE GENITAL SYSTEM
PROGESTOGENS AND ESTROGENS IN COMBINATION
Progestogens and estrogens, sequential preparations
ATC L02AB01 ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
ENDOCRINE THERAPY
HORMONES AND RELATED AGENTS
Progestogens
FDA CS M0447349 Progesterone Congeners
MeSH PA D000970 Antineoplastic Agents
MeSH PA D018931 Antineoplastic Agents, Hormonal
MeSH PA D003270 Contraceptive Agents
MeSH PA D003271 Contraceptive Agents, Female
MeSH PA D000080066 Contraceptive Agents, Hormonal
MeSH PA D003278 Contraceptives, Oral, Hormonal
MeSH PA D003280 Contraceptives, Oral, Synthetic
MeSH PA D012102 Reproductive Control Agents
CHEBI has role CHEBI:35610 antineoplastic agents
CHEBI has role CHEBI:49323 contraceptive drugs
CHEBI has role CHEBI:49326 synthetic oral contraceptives
CHEBI has role CHEBI:50779 appetite enhancing drug
CHEBI has role CHEBI:59826 progestins
FDA EPC N0000175602 Progestin
MeSH PA D019167 Appetite Stimulants
MeSH PA D002491 Central Nervous System Agents
MeSH PA D000697 Central Nervous System Stimulants

Drug Use | Suggest Off label Use Form| |View source of the data|

DiseaseRelationSNOMED_IDDOID
Endometrial carcinoma indication 254878006 DOID:2871
Hormone receptor positive malignant neoplasm of breast indication 417181009
Nutritional deficiency associated with AIDS indication 420691000
Cachexia due to HIV indication
Anorexia from HIV indication
Malignant tumor of ovary off-label use 363443007 DOID:2394
Hypertensive disorder contraindication 38341003 DOID:10763
Chronic heart failure contraindication 48447003
Male hypogonadism contraindication 48723006
Diabetes mellitus contraindication 73211009 DOID:9351
Hyperglycemia contraindication 80394007 DOID:4195
Kidney disease contraindication 90708001 DOID:557
Disease of liver contraindication 235856003 DOID:409
Pregnancy, function contraindication 289908002
Thromboembolic disorder contraindication 371039008
Adrenal cortical hypofunction contraindication 386584007 DOID:10493




๐Ÿถ Veterinary Drug Use

SpeciesUseRelation
Dogs Alleviation of false pregnancy Indication
Dogs Postponement of estrus Indication

๐Ÿถ Veterinary products

ProductApplicantIngredients
Ovaban Tablets 20 mg, Ovaban Tablets 5 mg Intervet Inc. 1

Acid dissociation constants calculated using MoKa v3.0.0

None

Orange Book patent data (new drug applications)

Formulation strengthTrade nameApplicantApplication numberApproval dateTypeDose formRoutePatent numberPatent expiration datePatent use
125MG/ML MEGACE ES ENDO PHARMS INC N021778 July 5, 2005 RX SUSPENSION ORAL 7101576 April 22, 2024 TREATMENT OF ANOREXIA, CACHEXIA, OR AN UNEXPLAINED, SIGNIFICANT WEIGHT LOSS IN PATIENTS WITH A DIAGNOSIS OF ACQUIRED IMMUNODEFICIENCY SYNDROME (AIDS)
125MG/ML MEGACE ES ENDO PHARMS INC N021778 July 5, 2005 RX SUSPENSION ORAL 9040088 April 22, 2024 TREATMENT OF ANOREXIA, CACHEXIA, OR AN UNEXPLAINED, SIGNIFICANT WEIGHT LOSS IN PATIENTS WITH A DIAGNOSIS OF ACQUIRED IMMUNODEFICIENCY SYNDROME (AIDS)
125MG/ML MEGACE ES ENDO PHARMS INC N021778 July 5, 2005 RX SUSPENSION ORAL 9101540 April 22, 2024 TREATMENT OF ANOREXIA, CACHEXIA, OR AN UNEXPLAINED, SIGNIFICANT WEIGHT LOSS IN PATIENTS WITH A DIAGNOSIS OF ACQUIRED IMMUNODEFICIENCY SYNDROME (AIDS)
125MG/ML MEGACE ES ENDO PHARMS INC N021778 July 5, 2005 RX SUSPENSION ORAL 9101549 April 22, 2024 TREATMENT OF ANOREXIA, CACHEXIA, OR AN UNEXPLAINED, SIGNIFICANT WEIGHT LOSS IN PATIENTS WITH A DIAGNOSIS OF ACQUIRED IMMUNODEFICIENCY SYNDROME (AIDS)
125MG/ML MEGACE ES ENDO PHARMS INC N021778 July 5, 2005 RX SUSPENSION ORAL 9107827 April 22, 2024 TREATMENT OF ANOREXIA, CACHEXIA, OR AN UNEXPLAINED, SIGNIFICANT WEIGHT LOSS IN PATIENTS WITH A DIAGNOSIS OF ACQUIRED IMMUNODEFICIENCY SYNDROME (AIDS)

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

TargetClassPharosUniProtActionTypeActivity value
(-log[M])
Mechanism
action
Bioact sourceMoA source
Progesterone receptor Nuclear hormone receptor AGONIST DRUGBANK CHEMBL
Multidrug resistance protein 1 Transporter WOMBAT-PK
Glucocorticoid receptor Nuclear hormone receptor Ki 8.06 DRUG MATRIX
Cytochrome P450 2C9 Enzyme IC50 5 DRUG MATRIX
Androgen receptor Transcription factor Ki 7.70 DRUG MATRIX
Progesterone receptor Transcription factor Ki 8.84 DRUG MATRIX

External reference:

IDSource
4022205 VUID
N0000020211 NUI
D00952 KEGG_DRUG
4018133 VANDF
4022205 VANDF
C0065879 UMLSCUI
CHEBI:6723 CHEBI
CHEBI:6722 CHEBI
CHEMBL1201139 ChEMBL_ID
DB00351 DRUGBANK_ID
D019290 MESH_DESCRIPTOR_UI
11683 PUBCHEM_CID
TJ2M0FR8ES UNII
29451 RXNORM
1784 MMSL
5036 MMSL
d01348 MMSL
002667 NDDF
004823 NDDF
126091007 SNOMEDCT_US
126092000 SNOMEDCT_US
38578004 SNOMEDCT_US
C0025175 UMLSCUI
1529 INN_ID
3562-63-8 SECONDARY_CAS_RN
19090 PUBCHEM_CID
D008535 MESH_DESCRIPTOR_UI
9128 IUPHAR_LIGAND_ID
EA6LD1M70M UNII

Pharmaceutical products:

ProductCategoryIngredientsNDCFormQuantityRouteMarketingLabel
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 0121-0887 SUSPENSION 625 mg ORAL ANDA 30 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 0121-0945 SUSPENSION 400 mg ORAL ANDA 21 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 0121-4776 SUSPENSION 40 mg ORAL ANDA 24 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 0121-4776 SUSPENSION 40 mg ORAL ANDA 24 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 0121-4776 SUSPENSION 40 mg ORAL ANDA 24 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 0555-0606 TABLET 20 mg ORAL ANDA 20 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 0555-0607 TABLET 40 mg ORAL ANDA 20 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 0904-3571 TABLET 40 mg ORAL ANDA 19 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 0904-7072 SUSPENSION 40 mg ORAL ANDA 22 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 0904-7072 SUSPENSION 40 mg ORAL ANDA 22 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 0904-7236 TABLET 40 mg ORAL ANDA 17 sections
Megace ES HUMAN PRESCRIPTION DRUG LABEL 1 16590-254 SUSPENSION 125 mg ORAL NDA 11 sections
MEGESTOL HUMAN PRESCRIPTION DRUG LABEL 1 16590-898 SUSPENSION 40 mg ORAL ANDA 4 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 17856-0060 SUSPENSION 40 mg ORAL ANDA 12 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 17856-0907 SUSPENSION 40 mg ORAL ANDA 20 sections
Megace ES HUMAN PRESCRIPTION DRUG LABEL 1 17856-0949 SUSPENSION 125 mg ORAL NDA 25 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 24979-041 SUSPENSION 125 mg ORAL ANDA 27 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 24979-041 SUSPENSION 125 mg ORAL ANDA 27 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 33358-903 SUSPENSION 40 mg ORAL ANDA 10 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 49884-230 SUSPENSION 125 mg ORAL NDA AUTHORIZED GENERIC 26 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 49884-230 SUSPENSION 125 mg ORAL NDA AUTHORIZED GENERIC 26 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 49884-289 TABLET 20 mg ORAL ANDA 19 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 49884-289 TABLET 20 mg ORAL ANDA 19 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 49884-290 TABLET 40 mg ORAL ANDA 19 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 49884-290 TABLET 40 mg ORAL ANDA 19 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 49884-907 SUSPENSION 40 mg ORAL ANDA 22 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 49884-907 SUSPENSION 40 mg ORAL ANDA 22 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 49884-907 SUSPENSION 40 mg ORAL ANDA 22 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 50383-859 SUSPENSION 40 mg ORAL ANDA 19 sections
Megestrol Acetate HUMAN PRESCRIPTION DRUG LABEL 1 50383-859 SUSPENSION 40 mg ORAL ANDA 19 sections