Lomefloxacin
General information:
| Withdrawn ID: | 665 |
|---|---|
| Canonical SMILES: | |
| Standard InChI: | |
| Standard InChIKey: | |
| ATC class(es): | J01MA07 |
| S01AE04 | |
| Molecular Formula: | C17H19F2N3O3 |
| Molweight: | 351.348 |
Withdrawal information:
| Withdrawn due to drug safety reasons: | No |
|---|---|
| First approved: | 1992 |
| First withdrawn: | 2008 |
| Last withdrawn: | 2008 |
Side-effects:
| Total reported cases (submitted by medical professionals) with Lomefloxacin as primary suspect: | 5 |
|---|
Reported final outcomes:
| Disability: | 2 |
|---|---|
| Hospitalization (initial or prolonged): | 1 |
Reported side-effects:
| Side-effect | Case number |
|---|---|
| DELIRIUM | 1 |
| IMPAIRED WORK ABILITY | 1 |
| HEPATOCELLULAR DAMAGE | 1 |
| HEADACHE | 1 |
| GASTRIC BYPASS | 1 |
| EYE PAIN | 1 |
| ERYTHEMA MULTIFORME | 1 |
| ERYTHEMA | 1 |
| ERECTILE DYSFUNCTION | 1 |
| DRUG INEFFECTIVE | 1 |
| DIVERTICULITIS | 1 |
| INSOMNIA | 1 |
| DEAFNESS | 1 |
| BLOOD PRESSURE INCREASED | 1 |
| BLOOD GLUCOSE INCREASED | 1 |
| BLOOD CREATININE INCREASED | 1 |
| BACK PAIN | 1 |
| ATRIAL FIBRILLATION | 1 |
| ARTHRALGIA | 1 |
| ARRHYTHMIA | 1 |
| ANXIETY | 1 |
| AMNESIA | 1 |
| PROSTATIC OPERATION | 1 |
| TINNITUS | 1 |
| TENDON RUPTURE | 1 |
| SUNBURN | 1 |
| SPERM COUNT ZERO | 1 |
| SKIN DISCOLOURATION | 1 |
| SCAR | 1 |
| ROTATOR CUFF SYNDROME | 1 |
| RENAL DISORDER | 1 |
| RENAL CYST | 1 |
| PROSTATIC SPECIFIC ANTIGEN INCREASED | 1 |
| VISUAL ACUITY REDUCED | 1 |
| POSTOPERATIVE HERNIA | 1 |
| POST PROCEDURAL HAEMORRHAGE | 1 |
| PAIN IN JAW | 1 |
| PAIN IN EXTREMITY | 1 |
| PAIN | 1 |
| NEPHROLITHIASIS | 1 |
| MUSCLE SPASMS | 1 |
| JOINT INJURY | 1 |
| JAUNDICE CHOLESTATIC | 1 |
Toxicity information:
| Toxicity class: | 4 |
|---|---|
| Toxicity type: | N/A |
| LD50: | 1072 mg/kg |
External links:
| ChEBML: | CHEMBL561 |
|---|---|
| DrugBank: | DB00978 |