Drug Database
TR

tramadol (Qdolo)

✓ Approved

Athena Bioscience, LLC · Small Molecule · Small Molecule

What is tramadol?

tramadol is a small molecule developed by Athena Bioscience, LLC. It is approved for therapeutic indications via oral (po).

Drug Profile

Brand NamesQdolo
CompanyAthena Bioscience, LLC
Drug ClassSmall Molecule
RouteOral (PO)
StatusApproved

Therapeutic Indications

tramadol is developed for 1 unique indication across 1 therapeutic area.

Therapeutic AreaConditionPhase
Gastrointestinal disordersAbdominal pain✓ Approved

Related Research Articles

PubMedTurkish journal of medical sciences2026-07-25

Comparison of ultrasound-guided serratus posterior superior intercostal plane block and thoracic paravertebral block for postoperative analgesia after breast surgery: a prospective randomized noninferiority trial.

Kotanoğlu Mustafa Sırrı MS, Zengin Musa M, Küçük Onur O, Sezgi Atakan A et al.

This noninferiority trial aimed to evaluate whether the serratus posterior superior intercostal plane block (SPSIPB) provides noninferior postoperative analgesia compared with the thoracic paravertebral block (TPVB) after unilateral mastectomy. This prospective, randomized, assessor-blinded, parallel-group noninferiority trial enrolled 60 female patients scheduled for elective unilateral mastectomy. Patients received either ultrasound-guided SPSIPB (n = 30) or TPVB (n = 30) with 30 mL of 0.25% bupivacaine before induction. The primary outcome was visual analogue scale (VAS) pain scores (0-100 mm) at rest and during coughing over 24 h. Noninferiority was assessed using the Hodges-Lehmann median difference with 95% confidence intervals (CIs) and a prespecified margin of 13 mm, corresponding to the validated minimal clinically important difference (MCID). Secondary outcomes included opioid consumption, area under the curve (AUC) for cumulative pain burden, and patient satisfaction. All 60 patients completed the study. At the first postoperative hour, TPVB provided lower VAS scores at rest (median 10.0 vs. 23.0 mm, 95% CI of difference: 0 to 19). For resting VAS, noninferiority was demonstrated at 0 h, 4 h, and 24 h (upper bounds: 11.5 mm, 12.5 mm, and 5.0 mm). The 24-h AUC for resting VAS was comparable between groups (426 mm/h vs. 426.5 mm/h, p = 0.652). SPSIPB produced significantly lower tramadol consumption in the 12-to-24-h interval (median 0 vs. 50 mg, p < 0.001). However, total opioid consumption over the 24 h was comparable (p = 0.070). No block-related complications occurred in either group. Noninferiority of SPSIPB to TPVB was demonstrated for resting pain scores at the majority of postoperative time points after unilateral mastectomy. TPVB provided a transient early-phase analgesic advantage at 1 h and 2 h, while SPSIPB was associated with late-phase opioid sparing. The comparable cumulative pain burden across 24 h suggests that SPSIPB may serve as a periparavertebral alternative to TPVB when sustained analgesia and opioid reduction are clinical priorities.

PubMedEnvironmental monitoring and assessment2026-07-24

Wastewater-based assessment of episodic changes in psychoactive compounds and hormones during music festivals.

Tulipánová Alexandra A, Mackuľak Tomáš T, Horáková Ivana I, Imreová Zuzana Z et al.

This study investigated 11 psychoactive contaminants in wastewater influents at a municipal wastewater treatment plant in Slovakia between 2015 and 2018, based on 44 samples collected under regular conditions and an additional five samples collected during two music festivals in 2018. In addition, 17 progestagens were analyzed only in 2018 during festival days and their corresponding background days. Seasonal variation in normalized mass loads was generally minor, whereas interannual differences were more pronounced, particularly for psychoactive pharmaceuticals, which showed an overall decrease in 2018. Short-term but substantial increases in contaminant loads were observed during the festivals. During the multi-genre music festival, the normalized mass load of 3,4-methylenedioxymethamphetamine increased by more than 110-fold on the second festival day compared to the pre-festival average, while benzoylecgonine increased approximately 17-fold and dienogest by 1.3-fold. During the country/folk music festival, tramadol loads increased approximately twofold. Principal component analysis explained 70.75% of the total variance using the first two components and revealed a clear separation between festival and background samples. Overall, the results demonstrate that music festivals represent episodic pollution events capable of markedly altering wastewater influent composition over short time periods.

PubMedNigerian medical journal : journal of the Nigeria Medical Association2026-07-23

Opioid Addiction Medicine in Nigeria: Bridging Clinical Gaps in a Silent Epidemic-A Narrative Review.

Albert Ovie Martin OM

Opioid use disorder (OUD) is an emerging public-health challenge in Nigeria, driven largely by non-medical use of tramadol and codeine and compounded by limited access to evidence-based care. This narrative review synthesises evidence on the epidemiology, patterns, harms and treatment gaps for OUD in Nigeria and identifies priorities for policy and research. We searched PubMed/MEDLINE, Embase, PsycINFO, the Cochrane Library, African Journals Online, Google Scholar and grey literature from 2005 to 2024 for Nigerian data on non-medical opioid use, clinical harms, opioid agonist therapy (OAT) services, barriers and community supports. Findings were thematically synthesised using Braun and Clarke's framework, with quality appraisal using Joanna Briggs Institute tools and the SANRA scale. Thirty studies were included. The 2019 national drug use survey estimated past-year opioid use at 4.7% (approximately 4.6 million people), with institution-based surveys reporting high lifetime misuse among undergraduates. Reported harms included overdose, seizures, psychiatric comorbidity and injectable pentazocine dependence with severe soft-tissue infections. OAT availability remains highly centralised, with limited community recovery infrastructure. Nigeria's OUD burden is substantial but unevenly characterised, highlighting the need to decentralise OAT, integrate addiction training, strengthen surveillance and expand community supports.

PubMedJournal of forensic sciences2026-07-22

Forensic investigation of unexpected multi-drug overdoses: A case series suggesting potential homicidal poisoning.

Dinçer Bekir B, İğde Emre Nuri EN, Erkman Fatma Tuğba FT, Güler Fatih F et al.

Homicidal poisoning involving multiple prescription medications presents significant diagnostic challenges, particularly in determining intent. We present a case series of two unexpected deaths within the same social community, both linked to the same suspect. In Case 1, a 49-year-old woman found unresponsive was referred for forensic autopsy as a suspicious death. Although initial findings were non-specific, postmortem toxicological analysis revealed fatal multi-drug poisoning involving tramadol, diltiazem, and metoprolol. The investigation of Case 1 subsequently raised suspicion regarding Case 2, a 50-year-old woman originally certified as a natural death and buried without an autopsy. Following exhumation, toxicological evaluation of decomposed samples demonstrated exposure to tramadol, diltiazem, and metoprolol. Postmortem toxicological analysis was conducted at the Chemistry Specialization Department's ISO/IEC 17025-accredited laboratory, using advanced analytical techniques such as LC-MS/MS, liquid chromatography-time-of-flight mass spectrometry (LC-TOF-MS), and GC-MS. Review of both victims' medical histories revealed no records of prescriptions for tramadol, diltiazem, or metoprolol. The presence of a common suspect, absence of relevant medical prescriptions for either victim, and associated investigative findings supported third-party involvement, making homicidal poisoning highly probable, although the possibility of voluntary ingestion within a socially influenced context was also considered. This case series highlights the critical role of comprehensive toxicological analysis and multidisciplinary forensic evaluation in the reclassification of unexpected deaths. It underscores the importance of meticulous investigation to identify potential homicidal poisonings that may otherwise be misclassified as natural or undetermined.

PubMedJournal of cardiothoracic and vascular anesthesia2026-07-22

Evaluation of the Analgesic Efficacy of the Serratus Posterior Superior Intercostal Plane Block in Patients with Isolated Rib Fractures: A Case Series.

Gündoğdu Oğuz O, Avci O O, Ozbey M M, Dogan H H

To evaluate the analgesic efficacy of serratus posterior superior intercostal plane block (SPSIPB) in patients with isolated rib fractures. Retrospective single-center case series. Tertiary academic medical center. Seventeen adult patients with unilateral isolated rib fractures who were followed in the thoracic surgery department. All patients received ultrasound-guided single-shot SPSIPB, with the ultrasound probe positioned in the sagittal plane just medial to the medial border of the scapula and in-plane needle advancement in a caudocranial direction. A total of 30 mL of 0.25% bupivacaine with epinephrine was injected between the serratus posterior superior muscle and the second rib. Rescue analgesia with intravenous tramadol (50 mg) was administered when the Numeric Rating Scale (NRS) score was ≥4. Pain scores (NRS) were recorded before block application and at multiple time points up to 36 hours. Nine patients required no opioid consumption during follow-up, while five patients consumed 50 mg and three patients consumed 100 mg of tramadol. NRS scores decreased significantly after block application and remained low in most patients, with a tendency to increase at 36 hours. Dermatomal spread was predominantly between C5 and T8. SPSIPB may provide effective and prolonged analgesia in patients with isolated rib fractures. Its relatively consistent dermatomal spread and opioid-sparing profile suggest that it may serve as a safe and practical component of multimodal analgesia strategies; however, larger prospective comparative studies are needed to confirm these findings.

PubMedJournal of pain and symptom management2026-07-22

Small-Count Suppression Substantially Distorts Estimates of Pediatric Opioid Utilization in Japan.

Abe Kentaro K, Sugiyama Masanaka M, Miyazaki Kotone K, Sako Azumi A et al.

Effective pain management is essential for pediatric care. However, nationwide trends in pediatric opioid prescribing in Japan remain unclear because publicly available databases suppress small prescription quantities. To evaluate how small-count suppression influences the interpretation of pediatric opioid utilization estimates based on the National Database of Health Insurance Claims and Specific Health Checkups of Japan (NDB Open Data), with the secondary objective of describing nationwide prescribing trends. The NDB Open Data from fiscal years (FY) 2018-2023 were analyzed for children aged 0-14 years. Oral, transdermal, and suppository formulations of morphine, oxycodone, fentanyl, and tramadol were included; injectable formulations were excluded. Opioid utilization was converted to morphine milligram equivalents (MME) per 100,000 population. Prescription quantities below 1,000 units were coded as nondisclosure (ND) and treated as zero in the primary analysis. Sensitivity analyses imputed ND values using the estimated mean MME per reported unit. The suppression rate was defined as the proportion of strong opioid formulation categories with suppressed values. The suppression rate for the strong opioid formulation categories progressively increased and reached 100% in FY2023, indicating a substantial loss of observable prescription data. Sensitivity analyses demonstrated a 4.9-fold difference between the observed and imputed estimates in FY2022. In the primary analysis, estimated pediatric opioid utilization appeared to decrease from 1,826 to 346 mg MME/100,000 population between FY2018 and FY2023. Small-count suppression materially distorted estimates of pediatric opioid utilization derived from the NDB Open Data and may complicate the interpretation of prescribing trends in rare pediatric populations.

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