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This repository is under review for potential modification in compliance with Administration directives.

Details

Stereochemistry RACEMIC
Molecular Formula 3C15H13O3.Al
Molecular Weight 750.7673
Optical Activity ( + / - )
Defined Stereocenters 0 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FENOPROFEN ALUMINUM

SMILES

[Al+3].CC(C([O-])=O)C1=CC(OC2=CC=CC=C2)=CC=C1.CC(C([O-])=O)C3=CC(OC4=CC=CC=C4)=CC=C3.CC(C([O-])=O)C5=CC(OC6=CC=CC=C6)=CC=C5

InChI

InChIKey=MPLRWVOHWPDIJH-UHFFFAOYSA-K
InChI=1S/3C15H14O3.Al/c3*1-11(15(16)17)12-6-5-9-14(10-12)18-13-7-3-2-4-8-13;/h3*2-11H,1H3,(H,16,17);/q;;;+3/p-3

HIDE SMILES / InChI

Molecular Formula C15H13O3
Molecular Weight 241.2619
Charge -1
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula Al
Molecular Weight 26.9815386
Charge 3
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: Description was created based on several sources, including https://www.drugs.com/pro/fenoprofen.html

Fenoprofen is a propionic acid derivative with analgesic, antiinflammatory and antipyretic properties. Fenoprofen inhibits prostaglandin synthesis by decreasing the enzyme needed for biosynthesis. In patients with rheumatoid arthritis, the anti-inflammatory action of fenoprofen has been evidenced by relief of pain, increase in grip strength, and reductions in joint swelling, duration of morning stiffness, and disease activity (as assessed by both the investigator and the patient). In patients with osteoarthritis, the anti-inflammatory and analgesic effects of fenoprofen have been demonstrated by reduction in tenderness as a response to pressure and reductions in night pain, stiffness, swelling, and overall disease activity (as assessed by both the patient and the investigator). These effects have also been demonstrated by relief of pain with motion and at rest and increased range of motion in involved joints. In patients with rheumatoid arthritis and osteoarthritis, clinical studies have shown fenoprofen to be comparable to aspirin in controlling the aforementioned measures of disease activity, but mild gastrointestinal reactions (nausea, dyspepsia) and tinnitus occurred less frequently in patients treated with fenoprofen than in aspirin-treated patients. It is not known whether fenoprofen causes less peptic ulceration than does aspirin. In patients with pain, the analgesic action of fenoprofen has produced a reduction in pain intensity, an increase in pain relief, improvement in total analgesia scores, and a sustained analgesic effect. Indicated for relief of the signs and symptoms of rheumatoid arthritis and osteoarthritis. Also for the relief of mild to moderate pain.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
NALFON

Approved Use

NALFON is a nonsteroidal anti-inflammatory drug indicated for: • Relief of mild to moderate pain in adults. • Relief of the signs and symptoms of rheumatoid arthritis. • Relief of the signs and symptoms of osteoarthritis.

Launch Date

1976
Primary
NALFON

Approved Use

NALFON is a nonsteroidal anti-inflammatory drug indicated for: • Relief of mild to moderate pain in adults. • Relief of the signs and symptoms of rheumatoid arthritis. • Relief of the signs and symptoms of osteoarthritis.

Launch Date

1976
Primary
NALFON

Approved Use

NALFON is a nonsteroidal anti-inflammatory drug indicated for: • Relief of mild to moderate pain in adults. • Relief of the signs and symptoms of rheumatoid arthritis. • Relief of the signs and symptoms of osteoarthritis.

Launch Date

1976
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
28.3 μg/mL
300 mg single, oral
dose: 300 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
FENOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
105.2 μg × h/mL
300 mg single, oral
dose: 300 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
FENOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
3 h
300 mg single, oral
dose: 300 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
FENOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
Funbound

Funbound

ValueDoseCo-administeredAnalytePopulation
1%
300 mg single, oral
dose: 300 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
FENOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
Doses

Doses

DosePopulationAdverse events​
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Disc. AE: Reaction gastrointestinal, Reaction skin...
Other AEs: Dyspepsia, Nausea...
AEs leading to
discontinuation/dose reduction:
Reaction gastrointestinal (2%)
Reaction skin (1%)
Cardiovascular disorder (NOS) (0.5%)
Other AEs:
Dyspepsia (10%)
Nausea (7.7%)
Constipation (7%)
Vomiting (2.6%)
Abdominal pain (2%)
Diarrhea (1.8%)
Headache (8.7%)
Somnolence (8.5%)
Dizziness (6.5%)
Tremor (2.2%)
Confusion (1.4%)
Sweating increased (4.6%)
Pruritus (4.2%)
Rash (3.7%)
Tinnitus (4.5%)
Blurred vision (2.2%)
Hearing decreased (1.6%)
Palpitations (2.5%)
Nervousness (5.7%)
Asthenia (5.4%)
Peripheral edema (5%)
Dyspnea (2.8%)
Fatigue (1.7%)
Upper respiratory infection (1.5%)
Nasopharyngitis (1.2%)
Gastritis (<1%)
Ulcer peptic with perforation (<1%)
Ulcer peptic with perforation (<1%)
Gastrointestinal hemorrhage (<1%)
Anorexia (<1%)
Flatulence (<1%)
Dry mouth (<1%)
Blood in stool (<1%)
Alkaline phosphatase increased (<1%)
LDH increased (<1%)
SGOT increased (<1%)
Jaundice (<1%)
Cholestatic hepatitis (<1%)
Buccal mucosa aphthous ulceration (<1%)
Taste metallic (<1%)
Pancreatitis (<1%)
Atrial fibrillation (<1%)
Pulmonary edema (<1%)
Electrocardiogram change (<1%)
Supraventricular tachycardia (<1%)
Renal failure (<1%)
Dysuria (<1%)
Cystitis (<1%)
Hematuria (<1%)
Oliguria (<1%)
Azotemia (<1%)
Anuria (<1%)
Nephritis interstitial (<1%)
Nephrosis (<1%)
Acute papillary necrosis (<1%)
Angioedema (<1%)
Purpura (<1%)
Bruising (<1%)
Hemorrhage (<1%)
Thrombocytopenia (<1%)
Hemolytic anemia (<1%)
Aplastic anemia (<1%)
Agranulocytosis (<1%)
Pancytopenia (<1%)
Depression (<1%)
Disorientation (<1%)
Seizures (<1%)
Trigeminal neuralgia (<1%)
Burning tongue (<1%)
Diplopia (<1%)
Optic neuritis (<1%)
Exfoliative dermatitis (<1%)
Toxic epidermal necrolysis (<1%)
Stevens-Johnson syndrome (<1%)
Alopecia (<1%)
Anaphylaxis (<1%)
Urticaria (<1%)
Malaise (<1%)
Insomnia (<1%)
Tachycardia (<1%)
Personality change (<1%)
Lymphadenopathy (<1%)
Mastodynia (<1%)
Fever (<1%)
Sources:
AEs

AEs

AESignificanceDosePopulation
Cardiovascular disorder (NOS) 0.5%
Disc. AE
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Reaction skin 1%
Disc. AE
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Nasopharyngitis 1.2%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Confusion 1.4%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Upper respiratory infection 1.5%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Hearing decreased 1.6%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Fatigue 1.7%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Diarrhea 1.8%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Dyspepsia 10%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Abdominal pain 2%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Reaction gastrointestinal 2%
Disc. AE
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Blurred vision 2.2%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Tremor 2.2%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Palpitations 2.5%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Vomiting 2.6%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Dyspnea 2.8%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Rash 3.7%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Pruritus 4.2%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Tinnitus 4.5%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Sweating increased 4.6%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Peripheral edema 5%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Asthenia 5.4%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Nervousness 5.7%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Dizziness 6.5%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Constipation 7%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Nausea 7.7%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Somnolence 8.5%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Headache 8.7%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Acute papillary necrosis <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Agranulocytosis <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Alkaline phosphatase increased <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Alopecia <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Anaphylaxis <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Angioedema <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Anorexia <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Anuria <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Aplastic anemia <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Atrial fibrillation <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Azotemia <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Blood in stool <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Bruising <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Buccal mucosa aphthous ulceration <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Burning tongue <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Cholestatic hepatitis <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Cystitis <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Depression <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Diplopia <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Disorientation <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Dry mouth <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Dysuria <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Electrocardiogram change <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Exfoliative dermatitis <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Fever <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Flatulence <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Gastritis <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Gastrointestinal hemorrhage <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Hematuria <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Hemolytic anemia <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Hemorrhage <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Insomnia <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Jaundice <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
LDH increased <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Lymphadenopathy <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Malaise <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Mastodynia <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Nephritis interstitial <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Nephrosis <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Oliguria <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Optic neuritis <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Pancreatitis <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Pancytopenia <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Personality change <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Pulmonary edema <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Purpura <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Renal failure <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
SGOT increased <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Seizures <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Stevens-Johnson syndrome <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Supraventricular tachycardia <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Tachycardia <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Taste metallic <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Thrombocytopenia <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Toxic epidermal necrolysis <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Trigeminal neuralgia <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Ulcer peptic with perforation <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Ulcer peptic with perforation <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
Urticaria <1%
400 mg 3 times / day steady, oral
Recommended
Dose: 400 mg, 3 times / day
Route: oral
Route: steady
Dose: 400 mg, 3 times / day
Sources:
unhealthy
PubMed

PubMed

TitleDatePubMed
Thioesterification of 2-arylpropionic acids by recombinant acyl-coenzyme A synthetases (ACS1 and ACS2).
2000 Apr
Risk of upper gastrointestinal bleeding and perforation associated with low-dose aspirin as plain and enteric-coated formulations.
2001
Dehydration, hydration behavior, and structural analysis of fenoprofen calcium.
2001 Jul
Enantioselective inhibition of the binding of rac-profens to human serum albumin induced by lithocholate.
2001 Jul
Macromolecular prodrugs. IX. Synthesis of polymer-fenoprofen conjugates.
2001 Oct 9
Capillary electrochromatographic separation of non-steroidal anti-inflammatory drugs with a histidine bonded phase.
2002 Dec 27
Prediction of selectivity for enantiomeric separations of uncharged compounds by capillary electrophoresis involving dual cyclodextrin systems.
2002 Mar 1
Renal papillary necrosis.
2002 Nov-Dec
Enhancement of selectivity and resolution in the enantioseparation of uncharged compounds using mixtures of oppositely charged cyclodextrins in capillary electrophoresis.
2003 Jan
Risk of cancer in a large cohort of nonaspirin NSAID users: a population-based study.
2003 Jun 2
Hyaluronidase inhibitors (sodium cromoglycate and sodium auro-thiomalate) reduce the local tissue damage and prolong the survival time of mice injected with Naja kaouthia and Calloselasma rhodostoma venoms.
2003 Nov
Capillary electrophoresis with laser induced-fluorescence detection of profens derivatized with the water-soluble fluorogenic reagent 4-N-(4-N'-aminoethyl)piperazino-7-nitro-2,1,3-benzoxadiazole.
2003 Sep 5
Risk of breast cancer among users of aspirin and other anti-inflammatory drugs.
2004 Aug 2
Optimization of sample stacking for the simultaneous determination of nonsteroidal anti-inflammatory drugs with a wall-coated histidine capillary column.
2004 Feb
Gastrointestinally distributed UDP-glucuronosyltransferase 1A10, which metabolizes estrogens and nonsteroidal anti-inflammatory drugs, depends upon phosphorylation.
2004 Jul 2
Enantioselective kinetic disposition of fenoprofen in rats with experimental diabetes or adjuvant-induced arthritis.
2004 Oct
Using terahertz pulsed spectroscopy to quantify pharmaceutical polymorphism and crystallinity.
2005 Apr
Determination of nonsteroidal antiinflammatory drugs in water samples using liquid chromatography coupled with diode-array detector and mass spectrometry.
2005 Nov
Non-steroidal anti-inflammatory agents for cystoid macular oedema following cataract surgery: a systematic review.
2005 Nov
Long-term use of non-steroidal anti-inflammatory drugs and the risk of myocardial infarction in the general population.
2005 Nov 29
Antioxidant activity and inhibition of human neutrophil oxidative burst mediated by arylpropionic acid non-steroidal anti-inflammatory drugs.
2006 Aug
Vancomycin as chiral selector for enantioselective separation of selected profen nonsteroidal anti-inflammatory drugs in capillary liquid chromatography.
2006 Aug
Determination of acidic drugs and caffeine in municipal wastewaters and receiving waters by gas chromatography-ion trap tandem mass spectrometry.
2006 May 26
Pharmacodynamics, chiral pharmacokinetics, and pharmacokinetic-pharmacodynamic modeling of fenoprofen in patients with diabetes mellitus.
2006 Nov
Synthesis and in vitro antitumor effect of diclofenac and fenoprofen thiolated and nonthiolated polyaspartamide-drug conjugates.
2007 Jan
Rapid online-SPE-MS/MS method for ketoprofen determination in dermal interstitial fluid samples from rats obtained by microdialysis or open-flow microperfusion.
2007 May 1
Combined use of chiral ionic liquid and CD for MEKC: Part II. Determination of binding constants.
2009 Aug
Antioxidant activity of NSAID hydroxamic acids.
2009 Jun
Ibuprofen-arginine generates nitric oxide and has enhanced anti-inflammatory effects.
2009 Oct
Aldosterone glucuronidation by human liver and kidney microsomes and recombinant UDP-glucuronosyltransferases: inhibition by NSAIDs.
2009 Sep
A protein-coated magnetic beads as a tool for the rapid drug-protein binding study.
2010 Jul 8
Cyclooxygenase Inhibitors, Aspirin and Ibuprofen, Inhibit MHC-restricted Antigen Presentation in Dendritic Cells.
2010 Jun
Patents

Sample Use Guides

In Vivo Use Guide
400 mg to 600 mg orally 3 or 4 times a day -Maximum dose: 3200 mg/day
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 23:26:44 GMT 2025
Edited
by admin
on Mon Mar 31 23:26:44 GMT 2025
Record UNII
R56740U8WB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FENOPROFEN ALUMINUM
Common Name English
BENZENEACETIC ACID, .ALPHA.-METHYL-3-PHENOXY-, ALUMINUM SALT
Preferred Name English
FENOPROFEN ALUMINIUM
Common Name English
BENZENEACETIC ACID, .ALPHA.-METHYL-3-PHENOXY-, ALUMINUM SALT (3:1)
Systematic Name English
Code System Code Type Description
PUBCHEM
126961359
Created by admin on Mon Mar 31 23:26:44 GMT 2025 , Edited by admin on Mon Mar 31 23:26:44 GMT 2025
PRIMARY
FDA UNII
R56740U8WB
Created by admin on Mon Mar 31 23:26:44 GMT 2025 , Edited by admin on Mon Mar 31 23:26:44 GMT 2025
PRIMARY
CAS
101623-39-6
Created by admin on Mon Mar 31 23:26:44 GMT 2025 , Edited by admin on Mon Mar 31 23:26:44 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY