ciprofloxacine
      J - Antiinfectives For Systemic Use -> J01 - Antibacterials For Systemic Use -> J01M - Quinolone Antibacterials -> J01MA - Fluoroquinolones -> J01MA02 - Ciprofloxacin
    
          
        Administration category:
         Free
      
    
          
        Medicine group:
        antibacterial
      
    
    
          
        Brand name:
                  Ciproxin
              
      Safety margins
| Weight | ROA | Dosage | |
|---|---|---|---|
| 
                                                      ROA: po  | 
                        
                                                      Dosage: 500mg 2 dd to max. 750mg 2 dd  | 
                      ||
| 
                                                      ROA: iv  | 
                        
                                                      Dosage: 400mg 2 dd to max. 400mg 3 dd  | 
                      ||
| 
                          Comments:
                                                       Bij botinfecties, infecties met Pseudomonas species of infecties met intermediaire gevoelige micro-organismen hoog doseren (2 dd 750 mg p.o. of 3 dd 400 mg i.v.).  | 
                      |||
Dosage for "I" sensitivity
| Weight | ROA | Load | Dosage | 
|---|---|---|---|
| 
                                                      ROA: po  | 
                        
                          Load: -  | 
                        
                                                      Dosage: 750mg 2 dd  | 
                      |
| 
                                                      ROA: iv  | 
                        
                          Load: -  | 
                        
                                                      Dosage: 400mg 3 dd  | 
                      
Kidney function
| ROA | GFR | Dosage | Interval | Comments | 
|---|---|---|---|---|
| ROA: po | ||||
| 
                                                      GFR: 10 - 30  | 
                        
                                                      Interval: 24 Hours  | 
                        
                                                      Comments: 1 dd 500 - 750 mg p.o.. Bij ernstig ziek 2 dd 500 -750 mg.  | 
                      ||
| 
                                                      GFR: <10  | 
                        
                                                      Interval: 24 Hours  | 
                        
                                                      Comments: 1 dd 500 mg p.o.  | 
                      ||
| ROA: iv | ||||
| 
                                                      GFR: 10 - 30  | 
                        
                                                      Interval: 24 Hours  | 
                        
                                                      Comments: 1 dd 400 mg i.v.. Bij ernstig ziek 2 dd 400 mg i.v.  | 
                      ||
| 
                                                      GFR: <10  | 
                        
                                                      Interval: 24 Hours  | 
                        
                                                      Comments: 1 dd 400 mg i.v.  | 
                      ||
Notes GFR general:
Bij eGFR 10-30: Bij botinfecties, infecties met Pseudomonas species of infecties met intermediaire gevoelige micro-organismen hoog doseren (2 dd 750 mg p.o. of 2 dd 400 mg i.v.). 
            
              
                Renal elimination: 
                40-70%
              
            
                    
                                
              
                Dosage: 
                dependent on kidney function
              
            
                    
        Renal function-replacement therapy
CAPD: 1dd 400 mg i.v. of 1 dd 500 mg per os. Indien ernstig ziek 2dd 400 mg i.v. of 2 dd 500 mg p.o.
Hemo dialysis: 1dd 400 mg i.v. of 1 dd 500 mg per os. Indien ernstig ziek 2dd 400 mg i.v. of 2 dd 500 mg p.o.
CAV / VVHD: Normale dosering toepassen.
Interactions
| Interaction with (ATC): | Interaction with: | Expected effect: | 
|---|---|---|
| 
                    Interaction with (ATC): R03DA04 - Theophylline  | 
                
                                  
                    Interaction with: | 
                
                                  
                    Expected effect: verhoging plasmaconcentratie theofylline  | 
                
              
| 
                    Interaction with (ATC): | 
                
                                  
                    Interaction with: ijzerzouten  | 
                
                                  
                    Expected effect: vermindering absorptie ciprofloxacine  | 
                
              
| 
                    Interaction with (ATC): | 
                
                                  
                    Interaction with: aluminium- of magnesium bevattende antacida  | 
                
                                  
                    Expected effect: vermindering absorptie ciprofloxacine  | 
                
              
| 
                    Interaction with (ATC): A02BX02 - Sucralfate  | 
                
                                  
                    Interaction with: | 
                
                                  
                    Expected effect: vermindering absorptie ciprofloxacine  | 
                
              
Pregnancy
Due to the expiration of the alphanumeric classification for use in pregnancy and lactation, reference is made to the current, online information of the Teratology Information Service (TIS) of LAREB:
- http://www.lareb.nl//Teratologie/Naslagwerk-GZB/GZB---Zwangerschap#TOC_Middelen_bij6
 - http://www.lareb.nl//Teratologie/Naslagwerk-GZB/GZB---Borstvoeding#TOC_Middelen_bij16
 
          
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      Metadata
            Swab vid: M-501829.1
            Updated: 09/08/2023 - 12:12
            Status: Published
          
          
General comments
Bij nierfunctiestoornissen of nierfunctievervangende therapie eventueel doseren op geleide van de ciprofloxacineconcentratie.