| 5-FU + leucovorin |
Pancreatic adenocarcinoma |
H |
SP2 |
Miner |
0.537 |
Transform |
Chemotherapy |
|
| 5-FU/Capecitabine |
Gastric/GEJ |
H |
SP2 |
Architect |
0.300 |
Transform |
Antimetabolite |
|
| 5-FU/leucovorin |
Colorectal (metastatic) |
H |
SP2 |
Miner |
0.593 |
Transform |
|
|
| 5-Fluorouracil |
Head & Neck Squamous Cell (HNSCC) |
H |
SP2 |
Architect |
0.450 |
Transform |
Antimetabolite |
|
| ADT (LHRH) |
Prostate (mCRPC) |
C |
SP1 |
Sentinel |
0.500 |
Prevent |
Hormonal |
|
| Abemaciclib |
Breast HR+/HER2− |
H |
SP2 |
Architect |
0.500 |
Transform |
CDK4/6 inhibitor |
|
| Abiraterone |
Prostate (mCRPC) |
C |
SP1 |
Sentinel |
0.721 |
Prevent |
Novel hormonal |
|
| Acarbose |
Type 2 Diabetes |
H |
SP3 |
Sentinel |
0.150 |
Alpha-glucosidase inhibition → delay glucose absorption |
Legacy |
|
| Adagrasib (KRAS G12C) |
Colorectal (metastatic) |
H |
SP2 |
Architect |
0.560 |
Transform |
|
|
| Adagrasib (KRAS G12C) |
NSCLC (non-squamous) |
C |
SP1 |
Architect |
0.600 |
Prevent |
|
|
| Aducanumab (discontinued) |
Alzheimer's Disease |
C |
SP1 |
Architect |
0.150 |
Transform |
Anti-amyloid mAb |
|
| Alectinib |
NSCLC (non-squamous) |
H |
SP2 |
Architect |
0.380 |
Transform |
Targeted (ALK) |
|
| Alpelisib |
Breast HR+/HER2− |
C |
SP3 |
Miner |
0.490 |
Regain control |
PI3K inhibitor |
|
| Amikacin |
Tuberculosis |
H |
SP2 |
Miner |
0.400 |
Ribosomal protein synthesis inhibition |
Group C |
|
| Amivantamab (EGFR exon20) |
NSCLC (non-squamous) |
C |
SP3 |
Catalyst |
0.420 |
Regain control |
|
|
| Anastrozole |
Breast HR+/HER2− |
C |
SP1 |
Sentinel |
0.558 |
Prevent |
Endocrine therapy |
|
| Apalutamide |
Prostate (mCRPC) |
H |
SP2 |
Sentinel |
0.716 |
Transform |
Novel hormonal |
|
| Atezolizumab |
Hepatocellular Carcinoma (HCC) |
C |
SP3 |
Sentinel |
0.350 |
Regain control |
ICI |
|
| Atezolizumab |
Melanoma |
C |
SP3 |
Sentinel |
0.615 |
Regain control |
|
|
| Atezolizumab |
NSCLC (non-squamous) |
C |
SP3 |
Sentinel |
0.575 |
Regain control |
Checkpoint inhibitor |
|
| Axitinib |
Renal cell carcinoma (clear cell) |
H |
SP2 |
Architect |
0.563 |
Transform |
|
|
| Bedaquiline |
Tuberculosis |
C |
SP2 |
Catalyst |
0.620 |
Inhibit ATP synthase |
Novel |
|
| Belzutifan |
Renal cell carcinoma (clear cell) |
H |
SP2 |
Architect |
0.600 |
Transform |
|
|
| Belzutifan (HIF-2α) |
Renal cell carcinoma (clear cell) |
C |
SP1 |
Architect |
0.580 |
Prevent |
|
|
| Bevacizumab |
Cervical Cancer |
H |
SP4 |
Observer |
0.520 |
Slow |
Anti-angiogenic |
|
| Bevacizumab |
Colorectal (metastatic) |
H |
SP4 |
Sentinel |
0.552 |
Slow |
|
|
| Bevacizumab |
Glioblastoma (GBM) |
C |
SP3 |
Sentinel |
0.705 |
Regain control |
Anti-angiogenic |
|
| Bevacizumab |
Hepatocellular Carcinoma (HCC) |
H |
SP4 |
Observer |
0.380 |
Slow |
Anti-angiogenic |
|
| Bevacizumab |
Melanoma |
H |
SP4 |
Sentinel |
0.520 |
Slow |
|
|
| Bevacizumab |
NSCLC (non-squamous) |
H |
SP4 |
Sentinel |
0.420 |
Slow |
Anti-angiogenic |
|
| Bevacizumab |
Ovarian (High-Grade Serous) |
H |
SP4 |
Observer |
0.520 |
Slow |
Anti-angiogenic |
|
| Bevacizumab |
Triple-Negative Breast Cancer |
H |
SP4 |
Observer |
0.450 |
Slow |
Anti-angiogenic |
|
| Binimetinib |
Melanoma |
H |
SP2 |
Architect |
0.586 |
Transform |
Targeted therapy |
|
| Bisoprolol |
Heart Failure |
H |
SP2 |
Sentinel |
0.420 |
Selective beta-1 blockade |
Pillar 2 |
|
| Blood pressure optimisation |
Alzheimer's Disease |
H |
SP4 |
Miner |
0.120 |
Consolidate |
Vascular |
|
| Broad-spectrum antibiotics |
Sepsis |
C |
SP1 |
Sentinel |
0.550 |
Prevent |
Antimicrobial |
|
| Cabazitaxel |
Prostate (mCRPC) |
H |
SP4 |
Miner |
0.683 |
Slow |
Chemotherapy |
|
| Cabozantinib |
Hepatocellular Carcinoma (HCC) |
H |
SP2 |
Architect |
0.548 |
Transform |
TKI |
|
| Cabozantinib |
Prostate (mCRPC) |
H |
SP4 |
Sentinel |
0.520 |
Slow |
|
|
| Cabozantinib |
Renal cell carcinoma (clear cell) |
H |
SP2 |
Sentinel |
0.554 |
Transform |
|
|
| Canagliflozin |
Type 2 Diabetes |
C |
SP3 |
Observer |
0.250 |
SGLT2 inhibition |
Preferred |
|
| Capecitabine |
Breast HR+/HER2− |
H |
SP2 |
Miner |
0.580 |
Transform |
Chemotherapy |
|
| Capecitabine |
Colorectal (metastatic) |
H |
SP2 |
Miner |
0.593 |
Transform |
|
|
| Carboplatin |
Breast HR+/HER2− |
H |
SP2 |
Miner |
0.450 |
Transform |
|
|
| Carboplatin |
Endometrial Cancer |
C |
SP1 |
Miner |
0.580 |
Prevent |
Platinum |
|
| Carboplatin |
NSCLC (non-squamous) |
H |
SP4 |
Miner |
0.528 |
Slow |
Chemotherapy |
|
| Carboplatin |
Ovarian (High-Grade Serous) |
C |
SP1 |
Miner |
0.620 |
Prevent |
Platinum |
|
| Carboplatin |
Triple-Negative Breast Cancer |
C |
SP1 |
Miner |
0.580 |
Prevent |
Platinum |
|
| Carvedilol |
Heart Failure |
H |
SP2 |
Sentinel |
0.440 |
Beta-1/2 + alpha-1 blockade |
Pillar 2 |
|
| Cetuximab |
Head & Neck Squamous Cell (HNSCC) |
H |
SP4 |
Observer |
0.550 |
Slow |
Targeted therapy |
|
| Cetuximab (KRAS WT) |
Colorectal (metastatic) |
C |
SP3 |
Sentinel |
0.568 |
Regain control |
|
|
| Cisplatin |
Cervical Cancer |
C |
SP1 |
Miner |
0.580 |
Prevent |
Platinum |
|
| Cisplatin |
Gastric/GEJ |
C |
SP1 |
Miner |
0.340 |
Prevent |
Platinum |
|
| Cisplatin |
Head & Neck Squamous Cell (HNSCC) |
C |
SP1 |
Miner |
0.600 |
Prevent |
Platinum |
|
| Cisplatin |
NSCLC (non-squamous) |
H |
SP4 |
Miner |
0.520 |
Slow |
Chemotherapy |
|
| Cisplatin |
Ovarian (High-Grade Serous) |
C |
SP1 |
Miner |
0.600 |
Prevent |
Platinum |
|
| Cisplatin |
Urothelial/Bladder Cancer |
C |
SP1 |
Miner |
0.580 |
Prevent |
Platinum |
|
| Clofazimine |
Tuberculosis |
H |
SP3 |
Sentinel |
0.320 |
Generate reactive oxygen species |
Group B |
|
| Cobimetinib |
Melanoma |
H |
SP2 |
Architect |
0.580 |
Transform |
|
|
| Crizotinib |
NSCLC (non-squamous) |
H |
SP2 |
Architect |
0.390 |
Transform |
|
|
| Crystalloid resuscitation (30mL/kg) |
Sepsis |
H |
SP2 |
Miner |
0.400 |
Provoke |
Fluid |
|
| Cycloserine |
Tuberculosis |
H |
SP4 |
Sentinel |
0.220 |
Inhibit cell wall peptidoglycan |
Group B |
|
| Dabrafenib |
Melanoma |
H |
SP2 |
Architect |
0.673 |
Transform |
Targeted therapy |
|
| Dapagliflozin |
Heart Failure |
C |
SP4 |
Observer |
0.380 |
SGLT2 inhibition → osmotic diuresis + metabolic shift |
Pillar 4 |
|
| Dapagliflozin |
Type 2 Diabetes |
C |
SP3 |
Observer |
0.270 |
SGLT2 inhibition → glycosuria |
Preferred |
|
| Darolutamide |
Prostate (mCRPC) |
H |
SP2 |
Sentinel |
0.550 |
Transform |
Novel hormonal |
|
| Dato-DXd |
Breast HR+/HER2− |
C |
SP3 |
Catalyst |
0.520 |
Catalyse |
|
|
| Dato-DXd |
NSCLC (non-squamous) |
C |
SP3 |
Catalyst |
0.500 |
Catalyse |
|
|
| Delamanid |
Tuberculosis |
C |
SP1 |
Architect |
0.460 |
Inhibit mycolic acid synthesis |
Novel |
|
| Digoxin |
Heart Failure |
H |
SP3 |
Sentinel |
0.160 |
Na/K-ATPase inhibition → inotropy |
Legacy |
|
| Dobutamine |
Heart Failure |
C |
SP3 |
Catalyst |
0.120 |
Beta-1 agonist → contractility |
Acute |
|
| Docetaxel |
Head & Neck Squamous Cell (HNSCC) |
H |
SP2 |
Architect |
0.500 |
Transform |
Taxane |
|
| Docetaxel |
NSCLC (non-squamous) |
H |
SP2 |
Miner |
0.350 |
Transform |
Chemotherapy |
|
| Docetaxel |
Prostate (mCRPC) |
H |
SP4 |
Miner |
0.719 |
Slow |
Chemotherapy |
|
| Donanemab (Kisunla) |
Alzheimer's Disease |
C |
SP1 |
Architect |
0.350 |
Transform |
Anti-amyloid mAb |
|
| Donepezil (Aricept) |
Alzheimer's Disease |
H |
SP3 |
Sentinel |
0.250 |
Prevent |
Cholinesterase inhibitor |
|
| Dostarlimab |
Endometrial Cancer |
C |
SP3 |
Sentinel |
0.650 |
Regain control |
Checkpoint inhibitor |
|
| Dulaglutide |
Type 2 Diabetes |
C |
SP1 |
Architect |
0.420 |
GLP-1 receptor agonism |
Established |
|
| Durvalumab |
Hepatocellular Carcinoma (HCC) |
C |
SP3 |
Sentinel |
0.420 |
Regain control |
ICI |
|
| Durvalumab |
NSCLC (non-squamous) |
C |
SP3 |
Sentinel |
0.580 |
Regain control |
Checkpoint inhibitor |
|
| Early enteral nutrition |
Sepsis |
H |
SP4 |
Catalyst |
0.200 |
Consolidate |
Supportive |
|
| Elacestrant |
Breast HR+/HER2− |
C |
SP1 |
Sentinel |
0.590 |
Prevent |
|
|
| Empagliflozin |
Heart Failure |
C |
SP4 |
Observer |
0.360 |
SGLT2 inhibition |
Pillar 4 |
|
| Empagliflozin |
Type 2 Diabetes |
C |
SP3 |
Observer |
0.270 |
SGLT2 inhibition |
Preferred |
|
| Enalapril |
Heart Failure |
H |
SP1 |
Sentinel |
0.360 |
ACE inhibition |
Pillar 1 (legacy) |
|
| Encorafenib |
Melanoma |
H |
SP2 |
Architect |
0.679 |
Transform |
Targeted therapy |
|
| Encorafenib (BRAF V600E) |
Colorectal (metastatic) |
H |
SP2 |
Architect |
0.769 |
Transform |
|
|
| Enfortumab vedotin |
Urothelial/Bladder Cancer |
C |
SP3 |
Catalyst |
0.721 |
Regain control |
ADC |
|
| Enzalutamide |
Prostate (mCRPC) |
H |
SP2 |
Sentinel |
0.706 |
Transform |
Novel hormonal |
|
| Eplerenone |
Heart Failure |
C |
SP3 |
Architect |
0.360 |
Selective MR antagonism |
Pillar 3 |
|
| Erdafitinib |
Urothelial/Bladder Cancer |
H |
SP4 |
Observer |
0.550 |
Slow |
Targeted therapy |
|
| Erlotinib |
Pancreatic adenocarcinoma |
C |
SP1 |
Architect |
0.320 |
Prevent |
|
|
| Ertugliflozin |
Type 2 Diabetes |
C |
SP3 |
Observer |
0.240 |
SGLT2 inhibition |
Established |
|
| Ethambutol |
Tuberculosis |
H |
SP2 |
Sentinel |
0.250 |
Inhibit arabinosyltransferase |
First-line |
|
| Ethionamide |
Tuberculosis |
H |
SP1 |
Sentinel |
0.250 |
Inhibit mycolic acid synthesis |
Second-line |
|
| Everolimus |
Breast HR+/HER2− |
H |
SP4 |
Miner |
0.050 |
Slow |
mTOR inhibitor |
|
| Everolimus |
Hepatocellular Carcinoma (HCC) |
H |
SP4 |
Observer |
0.200 |
Slow |
mTOR inhibitor |
|
| Everolimus |
Renal cell carcinoma (clear cell) |
H |
SP4 |
Miner |
0.605 |
Slow |
|
|
| Everolimus |
Renal cell carcinoma (clear cell) |
H |
SP4 |
Miner |
0.300 |
Slow |
|
|
| Exemestane |
Breast HR+/HER2− |
C |
SP1 |
Sentinel |
0.570 |
Prevent |
Endocrine therapy |
|
| Exenatide (weekly) |
Type 2 Diabetes |
C |
SP1 |
Architect |
0.360 |
GLP-1 receptor agonism |
Established |
|
| Finerenone |
Heart Failure |
C |
SP3 |
Architect |
0.280 |
Nonsteroidal selective MR antagonism |
Novel |
|
| Fruquintinib |
Colorectal (metastatic) |
H |
SP4 |
Sentinel |
0.530 |
Slow |
|
|
| Fulvestrant |
Breast HR+/HER2− |
C |
SP1 |
Sentinel |
0.505 |
Prevent |
Endocrine therapy |
|
| Furosemide |
Heart Failure |
H |
SP4 |
Sentinel |
0.150 |
Loop diuresis |
Symptomatic |
|
| Galantamine (Razadyne) |
Alzheimer's Disease |
H |
SP3 |
Sentinel |
0.200 |
Prevent |
Cholinesterase inhibitor |
|
| Gemcitabine |
Ovarian (High-Grade Serous) |
H |
SP2 |
Miner |
0.420 |
Transform |
Antimetabolite |
|
| Gemcitabine |
Pancreatic adenocarcinoma |
H |
SP2 |
Miner |
0.537 |
Transform |
Chemotherapy |
|
| Gemcitabine |
Urothelial/Bladder Cancer |
H |
SP2 |
Architect |
0.520 |
Transform |
Antimetabolite |
|
| Glimepiride |
Type 2 Diabetes |
H |
SP2 |
Miner |
0.400 |
Stimulate insulin secretion |
Legacy |
|
| Glyburide |
Type 2 Diabetes |
H |
SP2 |
Miner |
0.380 |
Stimulate insulin secretion |
Legacy |
|
| Hydralazine/Isosorbide |
Heart Failure |
H |
SP3 |
Sentinel |
0.320 |
Direct vasodilation + NO donor |
Alternative |
|
| Hydrocortisone (200mg/d) |
Sepsis |
H |
SP3 |
Architect |
0.350 |
Transform |
Corticosteroid |
|
| Hydrocortisone + Fludrocortisone |
Sepsis |
H |
SP3 |
Architect |
0.420 |
Transform |
Corticosteroid combo |
|
| IFN-γ (immunostimulation) |
Sepsis |
C |
SP3 |
Catalyst |
0.300 |
Catalyse |
Immunotherapy |
|
| IL-7 (lymphocyte recovery) |
Sepsis |
C |
SP3 |
Miner |
0.280 |
Provoke |
Immunotherapy |
|
| Imlunestrant |
Breast HR+/HER2− |
C |
SP1 |
Sentinel |
0.600 |
Prevent |
Endocrine therapy |
|
| Inavolisib |
Breast HR+/HER2− |
C |
SP3 |
Miner |
0.590 |
Regain control |
PI3K inhibitor |
|
| Insulin aspart |
Type 2 Diabetes |
H |
SP4 |
Miner |
0.350 |
Rapid-acting prandial insulin |
Essential |
|
| Insulin degludec |
Type 2 Diabetes |
H |
SP4 |
Sentinel |
0.410 |
Ultra-long-acting insulin replacement |
Essential |
|
| Insulin glargine |
Type 2 Diabetes |
H |
SP4 |
Sentinel |
0.430 |
Basal insulin replacement |
Essential |
|
| Insulin glargine U300 |
Type 2 Diabetes |
H |
SP4 |
Sentinel |
0.440 |
Concentrated ultra-long-acting basal insulin |
Essential |
|
| Ipilimumab |
Hepatocellular Carcinoma (HCC) |
C |
SP3 |
Sentinel |
0.360 |
Provoke |
ICI |
|
| Ipilimumab |
Melanoma |
C |
SP1 |
Sentinel |
0.563 |
Provoke |
Checkpoint inhibitor |
|
| Ipilimumab |
NSCLC (non-squamous) |
C |
SP1 |
Sentinel |
0.600 |
Provoke |
Checkpoint inhibitor |
|
| Ipilimumab |
Renal cell carcinoma (clear cell) |
C |
SP1 |
Sentinel |
0.524 |
Provoke |
|
|
| Irinotecan |
Colorectal (metastatic) |
C |
SP1 |
Miner |
0.598 |
Prevent |
|
|
| Irinotecan |
Pancreatic adenocarcinoma |
C |
SP1 |
Miner |
0.529 |
Prevent |
Chemotherapy |
|
| Isoniazid |
Tuberculosis |
H |
SP1 |
Sentinel |
0.580 |
Inhibit mycolic acid synthesis |
First-line |
|
| Ivabradine |
Heart Failure |
H |
SP2 |
Catalyst |
0.200 |
If channel inhibition → heart rate reduction |
Add-on |
|
| Lecanemab (Leqembi) |
Alzheimer's Disease |
C |
SP1 |
Architect |
0.270 |
Transform |
Anti-amyloid mAb |
|
| Lenvatinib |
Endometrial Cancer |
H |
SP4 |
Observer |
0.745 |
Slow |
Anti-angiogenic TKI |
|
| Lenvatinib |
Hepatocellular Carcinoma (HCC) |
C |
SP1 |
Sentinel |
0.430 |
Prevent |
TKI |
|
| Lenvatinib |
Melanoma |
H |
SP4 |
Sentinel |
0.580 |
Slow |
|
|
| Lenvatinib |
Renal cell carcinoma (clear cell) |
H |
SP2 |
Sentinel |
0.597 |
Transform |
|
|
| Letrozole |
Breast HR+/HER2− |
C |
SP1 |
Sentinel |
0.615 |
Prevent |
Endocrine therapy |
|
| Levofloxacin |
Tuberculosis |
C |
SP3 |
Architect |
0.440 |
Block DNA gyrase |
Group A |
|
| Linagliptin |
Type 2 Diabetes |
H |
SP1 |
Sentinel |
0.200 |
DPP-4 inhibition |
Established |
|
| Linezolid |
Tuberculosis |
H |
SP4 |
Miner |
0.480 |
Block protein synthesis |
Group A |
|
| Liraglutide |
Type 2 Diabetes |
C |
SP1 |
Architect |
0.450 |
GLP-1 receptor agonism |
Established |
|
| Lithium (microdose) |
Alzheimer's Disease |
H |
SP2 |
Miner |
0.150 |
Slow |
GSK-3β inhibitor |
|
| Lomustine |
Glioblastoma (GBM) |
H |
SP2 |
Architect |
0.676 |
Transform |
Alkylating |
|
| Lorlatinib |
NSCLC (non-squamous) |
H |
SP2 |
Architect |
0.370 |
Transform |
|
|
| Lorlatinib (ALK+) |
NSCLC (non-squamous) |
C |
SP1 |
Architect |
0.660 |
Prevent |
|
|
| Lu-PSMA-617 |
Prostate (mCRPC) |
C |
SP3 |
Catalyst |
0.930 |
Catalyse |
Radioligand |
|
| Masitinib (experimental) |
Alzheimer's Disease |
C |
SP3 |
Catalyst |
0.220 |
Catalyse |
Anti-inflammatory |
|
| Memantine (Namenda) |
Alzheimer's Disease |
H |
SP4 |
Sentinel |
0.200 |
Slow |
NMDA antagonist |
|
| Metformin |
Type 2 Diabetes |
H |
SP2 |
Sentinel |
0.380 |
Suppress hepatic glucose + improve insulin sensitivity |
Foundation |
|
| Metoprolol succinate |
Heart Failure |
H |
SP2 |
Sentinel |
0.400 |
Selective beta-1 blockade |
Pillar 2 |
|
| Milrinone |
Heart Failure |
C |
SP3 |
Catalyst |
0.100 |
PDE3 inhibition → inotropy + vasodilation |
Acute |
|
| Mirvetuximab soravtansine |
Ovarian (High-Grade Serous) |
C |
SP3 |
Catalyst |
0.550 |
Regain control |
ADC |
|
| Moxifloxacin |
Tuberculosis |
C |
SP3 |
Architect |
0.500 |
Block DNA gyrase |
Group A |
|
| Nab-paclitaxel |
Pancreatic adenocarcinoma |
H |
SP4 |
Miner |
0.539 |
Slow |
Chemotherapy |
|
| Nal-Irinotecan |
Pancreatic adenocarcinoma |
H |
SP2 |
Miner |
0.520 |
Transform |
|
|
| Nal-irinotecan |
Pancreatic adenocarcinoma |
C |
SP1 |
Miner |
0.540 |
Prevent |
|
|
| Niraparib |
Ovarian (High-Grade Serous) |
C |
SP3 |
Sentinel |
0.580 |
Regain control |
PARPi |
|
| Niraparib (HRR+) |
Prostate (mCRPC) |
H |
SP2 |
Miner |
0.560 |
Transform |
|
|
| Nitroglycerin |
Heart Failure |
H |
SP3 |
Sentinel |
0.100 |
Venodilation → preload reduction |
Acute |
|
| Nivolumab |
Gastric/GEJ |
C |
SP3 |
Sentinel |
0.270 |
Regain control |
Checkpoint inhibitor |
|
| Nivolumab |
Head & Neck Squamous Cell (HNSCC) |
C |
SP3 |
Sentinel |
0.753 |
Regain control |
Checkpoint inhibitor |
|
| Nivolumab |
Hepatocellular Carcinoma (HCC) |
C |
SP3 |
Sentinel |
0.460 |
Regain control |
ICI |
|
| Nivolumab |
Melanoma |
C |
SP3 |
Sentinel |
0.641 |
Regain control |
Checkpoint inhibitor |
|
| Nivolumab |
NSCLC (non-squamous) |
C |
SP3 |
Sentinel |
0.580 |
Regain control |
Checkpoint inhibitor |
|
| Nivolumab |
Renal cell carcinoma (clear cell) |
C |
SP3 |
Sentinel |
0.460 |
Regain control |
|
|
| Nivolumab (MSI-H) |
Colorectal (metastatic) |
C |
SP3 |
Sentinel |
0.580 |
Regain control |
|
|
| Norepinephrine |
Sepsis |
H |
SP2 |
Sentinel |
0.500 |
Prevent |
Vasopressor |
|
| Olaparib |
Ovarian (High-Grade Serous) |
C |
SP3 |
Sentinel |
0.720 |
Regain control |
PARPi |
|
| Olaparib |
Pancreatic adenocarcinoma |
H |
SP4 |
Miner |
0.569 |
Slow |
Targeted therapy |
|
| Olaparib |
Prostate (mCRPC) |
C |
SP3 |
Miner |
0.620 |
Regain control |
Targeted therapy |
|
| Olaparib |
Triple-Negative Breast Cancer |
C |
SP3 |
Sentinel |
0.550 |
Regain control |
PARPi |
|
| Olaparib (BRCA+) |
Pancreatic adenocarcinoma |
H |
SP2 |
Miner |
0.580 |
Transform |
|
|
| Omecamtiv mecarbil |
Heart Failure |
H |
SP4 |
Catalyst |
0.140 |
Cardiac myosin activator |
Novel |
|
| Osimertinib |
NSCLC (non-squamous) |
H |
SP2 |
Architect |
0.400 |
Transform |
Targeted (EGFR) |
|
| Oxaliplatin |
Colorectal (metastatic) |
H |
SP4 |
Miner |
0.603 |
Slow |
|
|
| Oxaliplatin |
Gastric/GEJ |
C |
SP1 |
Miner |
0.390 |
Prevent |
Platinum |
|
| Oxaliplatin |
Pancreatic adenocarcinoma |
C |
SP3 |
Miner |
0.529 |
Regain control |
Chemotherapy |
|
| PEG Liposomal Doxorubicin |
Ovarian (High-Grade Serous) |
H |
SP2 |
Architect |
0.480 |
Transform |
Anthracycline |
|
| Paclitaxel |
Cervical Cancer |
H |
SP2 |
Architect |
0.520 |
Transform |
Taxane |
|
| Paclitaxel |
Endometrial Cancer |
H |
SP2 |
Architect |
0.520 |
Transform |
Taxane |
|
| Paclitaxel |
Gastric/GEJ |
H |
SP2 |
Architect |
0.480 |
Transform |
Taxane |
|
| Paclitaxel |
NSCLC (non-squamous) |
H |
SP2 |
Miner |
0.540 |
Transform |
Chemotherapy |
|
| Paclitaxel |
Ovarian (High-Grade Serous) |
H |
SP2 |
Architect |
0.580 |
Transform |
Taxane |
|
| Paclitaxel (nab) |
Triple-Negative Breast Cancer |
H |
SP2 |
Architect |
0.550 |
Transform |
Taxane |
|
| Palbociclib |
Breast HR+/HER2− |
H |
SP2 |
Architect |
0.350 |
Transform |
CDK4/6 inhibitor |
|
| Panitumumab (KRAS WT) |
Colorectal (metastatic) |
C |
SP3 |
Sentinel |
0.568 |
Regain control |
|
|
| Para-aminosalicylic acid |
Tuberculosis |
H |
SP1 |
Sentinel |
0.180 |
Folate synthesis inhibition |
Group C |
|
| Pembrolizumab |
Breast HR+/HER2− |
C |
SP3 |
Sentinel |
0.380 |
Regain control |
|
|
| Pembrolizumab |
Cervical Cancer |
C |
SP3 |
Sentinel |
0.620 |
Regain control |
Checkpoint inhibitor |
|
| Pembrolizumab |
Endometrial Cancer |
C |
SP3 |
Sentinel |
0.600 |
Regain control |
Checkpoint inhibitor |
|
| Pembrolizumab |
Head & Neck Squamous Cell (HNSCC) |
C |
SP3 |
Sentinel |
0.580 |
Regain control |
Checkpoint inhibitor |
|
| Pembrolizumab |
Hepatocellular Carcinoma (HCC) |
C |
SP3 |
Sentinel |
0.583 |
Regain control |
ICI |
|
| Pembrolizumab |
Melanoma |
C |
SP3 |
Sentinel |
0.621 |
Regain control |
Checkpoint inhibitor |
|
| Pembrolizumab |
NSCLC (non-squamous) |
C |
SP3 |
Sentinel |
0.570 |
Regain control |
Checkpoint inhibitor |
|
| Pembrolizumab |
Ovarian (High-Grade Serous) |
C |
SP3 |
Sentinel |
0.350 |
Regain control |
Checkpoint inhibitor |
|
| Pembrolizumab |
Renal cell carcinoma (clear cell) |
C |
SP3 |
Sentinel |
0.460 |
Regain control |
|
|
| Pembrolizumab |
Triple-Negative Breast Cancer |
C |
SP3 |
Sentinel |
0.600 |
Regain control |
Checkpoint inhibitor |
|
| Pembrolizumab |
Urothelial/Bladder Cancer |
C |
SP3 |
Sentinel |
0.678 |
Regain control |
Checkpoint inhibitor |
|
| Pembrolizumab (MSI-H only) |
Colorectal (metastatic) |
C |
SP3 |
Sentinel |
0.659 |
Regain control |
|
|
| Pembrolizumab (MSI-H) |
Pancreatic adenocarcinoma |
C |
SP3 |
Sentinel |
0.550 |
Regain control |
|
|
| Pembrolizumab (MSI-H) |
Prostate (mCRPC) |
C |
SP3 |
Sentinel |
0.480 |
Regain control |
|
|
| Pemetrexed |
NSCLC (non-squamous) |
H |
SP2 |
Miner |
0.520 |
Transform |
Chemotherapy |
|
| Pioglitazone |
Type 2 Diabetes |
C |
SP2 |
Architect |
0.280 |
PPAR-gamma agonism |
Legacy |
|
| Pretomanid |
Tuberculosis |
C |
SP4 |
Catalyst |
0.540 |
Inhibit mycolic acid + anaerobic respiration |
Novel |
|
| Protective ventilation (lung-protective) |
Sepsis |
H |
SP4 |
Sentinel |
0.350 |
Slow |
Organ support |
|
| Pyrazinamide |
Tuberculosis |
C |
SP4 |
Observer |
0.550 |
Disrupt membrane energetics at acid pH |
First-line |
|
| Radium-223 |
Prostate (mCRPC) |
H |
SP4 |
Miner |
0.660 |
Slow |
|
|
| Radium-223 |
Prostate (mCRPC) |
H |
SP4 |
Miner |
0.550 |
Slow |
|
|
| Ramucirumab |
Gastric/GEJ |
H |
SP4 |
Observer |
0.250 |
Slow |
Anti-angiogenic |
|
| Ramucirumab |
Hepatocellular Carcinoma (HCC) |
H |
SP4 |
Observer |
0.551 |
Slow |
Anti-angiogenic |
|
| Ramucirumab |
NSCLC (non-squamous) |
H |
SP4 |
Sentinel |
0.380 |
Slow |
|
|
| Regorafenib |
Colorectal (metastatic) |
H |
SP2 |
Sentinel |
0.836 |
Transform |
|
|
| Regorafenib |
Hepatocellular Carcinoma (HCC) |
H |
SP2 |
Architect |
0.565 |
Transform |
TKI |
|
| Renal replacement therapy |
Sepsis |
H |
SP4 |
Miner |
0.250 |
Consolidate |
Organ support |
|
| Ribociclib |
Breast HR+/HER2− |
H |
SP2 |
Architect |
0.500 |
Transform |
CDK4/6 inhibitor |
|
| Rifampin |
Tuberculosis |
H |
SP2 |
Miner |
0.720 |
Block RNA polymerase |
First-line |
|
| Rifapentine |
Tuberculosis |
H |
SP2 |
Miner |
0.680 |
Block RNA polymerase |
First-line |
|
| Rivastigmine (Exelon) |
Alzheimer's Disease |
H |
SP3 |
Sentinel |
0.220 |
Prevent |
Cholinesterase inhibitor |
|
| Rucaparib |
Ovarian (High-Grade Serous) |
C |
SP3 |
Sentinel |
0.650 |
Regain control |
PARPi |
|
| Sacituzumab govitecan |
Breast HR+/HER2− |
C |
SP3 |
Catalyst |
0.530 |
Catalyse |
|
|
| Sacituzumab govitecan |
Triple-Negative Breast Cancer |
C |
SP3 |
Catalyst |
0.428 |
Regain control |
ADC |
|
| Sacubitril/Valsartan |
Heart Failure |
C |
SP1 |
Architect |
0.480 |
Neprilysin + AT1 receptor dual blockade |
Pillar 1 |
|
| Savolitinib |
Renal cell carcinoma (clear cell) |
H |
SP2 |
Architect |
0.550 |
Transform |
|
|
| Semaglutide |
Heart Failure |
C |
SP4 |
Architect |
0.220 |
GLP-1 RA → weight loss + metabolic improvement |
Novel |
|
| Semaglutide (injectable) |
Type 2 Diabetes |
C |
SP1 |
Architect |
0.520 |
GLP-1 receptor agonism |
Preferred |
|
| Semaglutide (oral) |
Type 2 Diabetes |
C |
SP1 |
Architect |
0.450 |
Oral GLP-1 receptor agonism |
Novel |
|
| Semorinemab (anti-tau) |
Alzheimer's Disease |
H |
SP2 |
Sentinel |
0.080 |
Prevent |
Anti-tau mAb |
|
| Sitagliptin |
Type 2 Diabetes |
H |
SP1 |
Sentinel |
0.220 |
DPP-4 inhibition |
Established |
|
| Sorafenib |
Hepatocellular Carcinoma (HCC) |
C |
SP1 |
Sentinel |
0.350 |
Prevent |
TKI |
|
| Sotorasib |
NSCLC (non-squamous) |
H |
SP2 |
Architect |
0.370 |
Transform |
Targeted (KRAS) |
|
| Sotorasib (KRAS G12C) |
Colorectal (metastatic) |
H |
SP2 |
Architect |
0.560 |
Transform |
|
|
| Source control (surgical/drainage) |
Sepsis |
C |
SP1 |
Architect |
0.450 |
Transform |
Surgical |
|
| Spartalizumab |
Melanoma |
C |
SP3 |
Sentinel |
0.520 |
Regain control |
|
|
| Spironolactone |
Heart Failure |
C |
SP3 |
Architect |
0.400 |
Mineralocorticoid receptor antagonism |
Pillar 3 |
|
| Streptomycin |
Tuberculosis |
H |
SP2 |
Miner |
0.380 |
Ribosomal protein synthesis inhibition |
Historical |
|
| Structured aerobic exercise |
Alzheimer's Disease |
C |
SP4 |
Catalyst |
0.150 |
Consolidate |
Lifestyle |
|
| Sunitinib |
Renal cell carcinoma (clear cell) |
H |
SP2 |
Architect |
0.538 |
Transform |
|
|
| T-DXd (HER2-low) |
Breast HR+/HER2− |
C |
SP3 |
Catalyst |
0.520 |
Catalyse |
ADC |
|
| T-VEC |
Melanoma |
C |
SP1 |
Catalyst |
0.550 |
Provoke |
Oncolytic |
|
| TAS-102 |
Colorectal (metastatic) |
H |
SP2 |
Miner |
0.280 |
Transform |
|
|
| TAS-102 (Lonsurf) |
Colorectal (metastatic) |
H |
SP2 |
Miner |
0.280 |
Transform |
|
|
| TTFields |
Glioblastoma (GBM) |
H |
SP4 |
Observer |
0.480 |
Slow |
Device |
|
| Tamoxifen |
Breast HR+/HER2− |
C |
SP1 |
Sentinel |
0.585 |
Prevent |
Endocrine therapy |
|
| Tebentafusp |
Melanoma |
C |
SP1 |
Catalyst |
0.550 |
Provoke |
|
|
| Temozolomide |
Glioblastoma (GBM) |
C |
SP1 |
Miner |
0.550 |
Prevent |
Alkylating |
|
| Temozolomide |
Melanoma |
H |
SP2 |
Miner |
0.420 |
Transform |
|
|
| Tiragolumab (anti-TIGIT) |
NSCLC (non-squamous) |
C |
SP1 |
Sentinel |
0.540 |
Provoke |
|
|
| Tirzepatide |
Type 2 Diabetes |
C |
SP1 |
Catalyst |
0.650 |
Dual GIP + GLP-1 receptor agonism |
Novel |
|
| Tivozanib |
Renal cell carcinoma (clear cell) |
H |
SP2 |
Sentinel |
0.449 |
Transform |
|
|
| Trametinib |
Melanoma |
H |
SP2 |
Architect |
0.591 |
Transform |
Targeted therapy |
|
| Trastuzumab |
Gastric/GEJ |
C |
SP3 |
Catalyst |
0.330 |
Regain control |
Targeted therapy |
|
| Tremelimumab |
Hepatocellular Carcinoma (HCC) |
C |
SP3 |
Sentinel |
0.280 |
Provoke |
ICI |
|
| Tremelimumab |
NSCLC (non-squamous) |
C |
SP1 |
Sentinel |
0.560 |
Provoke |
|
|
| Tucatinib |
Breast HR+/HER2− |
C |
SP1 |
Architect |
0.550 |
Prevent |
|
|
| Tucatinib (HER2+) |
Colorectal (metastatic) |
C |
SP3 |
Architect |
0.570 |
Regain control |
|
|
| Valsartan |
Heart Failure |
H |
SP1 |
Sentinel |
0.300 |
AT1 receptor blockade |
Pillar 1 (alt) |
|
| Vasopressin (add-on) |
Sepsis |
H |
SP2 |
Catalyst |
0.250 |
Accelerate |
Vasopressor |
|
| Vericiguat |
Heart Failure |
C |
SP3 |
Catalyst |
0.180 |
Soluble guanylate cyclase stimulation |
Novel |
|
| iGlarLixi (Soliqua) |
Type 2 Diabetes |
C |
SP4 |
Architect |
0.520 |
Fixed-ratio insulin + GLP-1 RA |
Combination |
|