Drug profile
Ciprofloxacin
Adult, child, renal, hepatic, pregnancy and breastfeeding information, with the source named on every line.
DRUG INFORMATION
ADULT
- No adult dose in this label - read the full label before dosing.
Source: Read and found silent: the US FDA label for ciprofloxacin (Ciprofloxacin),
retrieved 2026-08-29
CHILD
- Although effective in clinical trials, Ciprofloxacin is not a drug of first choice
in the pediatric population due to an increased incidence of adverse reactions
compared to controls. Quinolones, including Ciprofloxacin, cause arthropathy in
juvenile animals [see Warnings and Precautions ( 5.12 ) and Nonclinical Toxicology
( 13.2 )] .
Source: US FDA label for ciprofloxacin (Ciprofloxacin), section 'pediatric use',
retrieved 2026-08-29
RENAL IMPAIRMENT
- These alternative pathways of drug elimination appear to compensate for the
reduced renal excretion in patients with renal impairment.
Source: US FDA label for ciprofloxacin (Ciprofloxacin), section 'dosage and
administration', retrieved 2026-08-29
- Dosage guidelines for use in patients with renal impairment are shown in Table 4 .
Source: This line points to a numbered table that this card does not show - read
that table in the label before you dose. US FDA label for ciprofloxacin
(Ciprofloxacin), section 'dosage and administration', retrieved 2026-08-29
- In patients with severe infections and severe renal impairment, a unit dose of 750
mg may be administered at the intervals noted above.
Source: US FDA label for ciprofloxacin (Ciprofloxacin), section 'dosage and
administration', retrieved 2026-08-29
HEPATIC IMPAIRMENT
- Nonetheless, some modification of dosage is recommended, particularly for patients
with severe renal dysfunction [see Dosage and Administration ( 2.3 ) and Clinical
Pharmacology ( 12.3 )]. 8.7 Hepatic Impairment In preliminary studies in patients
with stable chronic liver cirrhosis, no significant changes in ciprofloxacin
pharmacokinetics have been observed.
Source: US FDA label for ciprofloxacin (Ciprofloxacin), section 'use in specific
populations', retrieved 2026-08-29
- The pharmacokinetics of ciprofloxacin in patients with acute hepatic
insufficiency, have not been studied.
Source: US FDA label for ciprofloxacin (Ciprofloxacin), section 'use in specific
populations', retrieved 2026-08-29
PREGNANCY [ AVOID ]
The label says not to use it. Read the quote below before deciding.
- Pregnancy Category C There are no adequate and well-controlled studies in pregnant
women.
Source: US FDA label for ciprofloxacin (Ciprofloxacin), section 'pregnancy',
retrieved 2026-08-29
- Ciprofloxacin should not be used during pregnancy unless the potential benefit
justifies the potential risk to both fetus and mother.
Source: US FDA label for ciprofloxacin (Ciprofloxacin), section 'pregnancy',
retrieved 2026-08-29
- An expert review of published data on experiences with ciprofloxacin use during
pregnancy by TERIS–the Teratogen Information System–concluded that therapeutic
doses during pregnancy are unlikely to pose a substantial teratogenic risk
(quantity and quality of data=fair), but the data are insufficient to state that
there is no risk.
Source: US FDA label for ciprofloxacin (Ciprofloxacin), section 'pregnancy',
retrieved 2026-08-29
BREASTFEEDING
- Ciprofloxacin is excreted in human milk.
Source: US FDA label for ciprofloxacin (Ciprofloxacin), section 'nursing mothers',
retrieved 2026-08-29
- The amount of ciprofloxacin absorbed by the nursing infant is unknown.
Source: US FDA label for ciprofloxacin (Ciprofloxacin), section 'nursing mothers',
retrieved 2026-08-29
- Because of the potential risk of serious adverse reactions (including articular
damage) in infants nursing from mothers taking Ciprofloxacin, a decision should be
made whether to discontinue nursing or to discontinue the drug, taking into
account the importance of the drug to the mother.
Source: US FDA label for ciprofloxacin (Ciprofloxacin), section 'nursing mothers',
retrieved 2026-08-29