Carboprost Tromethamine

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Carboprost Tromethamine
Generic name
CARBOPROST TROMETHAMINE
Manufacturer
Sagent Pharmaceuticals
Product type
HUMAN PRESCRIPTION DRUG
SPL set ID
ffc3a941-4d73-4273-a879-1565133a4d5d
SPL ID
8dcc3692-6db4-4b95-9ee9-c81db12c5d12
Version
1
Effective date
2025-12-02
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:57:16
Harmonized routes table
Harmonized routes
INTRAMUSCULAR

Boxed warning cross-check#

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Boxed warning sections page 1 of 1 · 1 matching rows.

boxed warning

WARNINGS Carboprost tromethamine injection sterile solution (carboprost tromethamine), like other potent oxytocic agents, should be used only with strict adherence to recommended dosages. Carboprost tromethamine injection should be used by medically trained personnel in a hospital which can provide immediate intensive care and acute surgical facilities.

Adverse reactions cross-check#

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adverse reactions

ADVERSE REACTIONS The adverse effects of carboprost tromethamine injection sterile solution are generally transient and reversible when therapy ends. The most frequent adverse reactions observed are related to its contractile effect on smooth muscle. In patients studied, approximately two-thirds experienced vomiting and diarrhea, approximately one-third had nausea, one-eighth had a temperature increase greater than 2° F, and one-fourteenth experienced flushing. The pretreatment or concurrent administration of antiemetic and antidiarrheal drugs decreases considerably the very high incidence of gastrointestinal effects common with all prostaglandins used for abortion. Their use should be considered an integral part of the management of patients undergoing abortion with carboprost tromethamine injection. Of those patients experiencing a temperature elevation, approximately one-sixteenth had a clinical diagnosis of endometritis. The remaining temperature elevations returned to normal within several hours after the last injection. Adverse effects observed during the use of carboprost tromethamine injection for abortion and for hemorrhage, not all of which are clearly drug related, in decreasing order of frequency include: Vomiting Nervousness Diarrhea Nosebleed Nausea Sleep disorders Flushing or hot flashes Dyspnea Chills or shivering Tightness in chest Coughing Wheezing Headaches Posterior cervical perforation Endometritis Weakness Hiccough Diaphoresis Dysmenorrhea-like pain Dizziness Paresthesia Blurred vision Backache Epigastric pain Muscular pain Excessive thirst Breast tenderness Twitching eyelids Eye pain Gagging, retching Drowsiness Dry throat Dystonia Sensation of choking Asthma Thyroid storm Injection site pain Syncope Tinnitus Palpitations Vertigo Rash Vaso-vagal syndrome Upper respiratory infection Dryness of mouth Leg cramps Hyperventilation Perforated uterus Respiratory distress Anxiety Hematemesis Chest pain Taste alterations Retained placental fragment Urinary tract infection Shortness of breath Septic shock Fullness of throat Torticollis Uterine sacculation Lethargy Faintness, light- headedness Hypertension Uterine rupture Tachycardia Pulmonary edema Endometritis from IUCD The most common complications when carboprost tromethamine injection was utilized for abortion requiring additional treatment after discharge from the hospital were endometritis, retained placental fragments, and excessive uterine bleeding, occurring in about one in every 50 patients. Post-marketing experience: Hypersensitivity reactions (e.g. Anaphylactic reaction, Anaphylactic shock, Anaphylactoid reaction, Angioedema). To report SUSPECTED ADVERSE REACTIONS, contact Sagent Pharmaceuticals at 1-866-625-1618 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch .

adverse reactions table

<table width="100%"><col width="50.000%" align="left"/><col width="50.000%" align="left"/><tbody><tr><td align="left" valign="top" styleCode="Toprule Botrule Lrule Rrule">Vomiting </td><td align="left" valign="top" styleCode="Toprule Botrule Rrule">Nervousness </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Diarrhea </td><td align="left" valign="top" styleCode="Botrule Rrule">Nosebleed </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Nausea </td><td align="left" valign="top" styleCode="Botrule Rrule">Sleep disorders </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Flushing or hot flashes </td><td align="left" valign="top" styleCode="Botrule Rrule">Dyspnea </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Chills or shivering </td><td align="left" valign="top" styleCode="Botrule Rrule">Tightness in chest </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Coughing </td><td align="left" valign="top" styleCode="Botrule Rrule">Wheezing </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Headaches </td><td align="left" valign="top" styleCode="Botrule Rrule">Posterior cervical perforation </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Endometritis </td><td align="left" valign="top" styleCode="Botrule Rrule">Weakness </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Hiccough </td><td align="left" valign="top" styleCode="Botrule Rrule">Diaphoresis </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Dysmenorrhea-like pain </td><td align="left" valign="top" styleCode="Botrule Rrule">Dizziness </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Paresthesia </td><td align="left" valign="top" styleCode="Botrule Rrule">Blurred vision </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Backache </td><td align="left" valign="top" styleCode="Botrule Rrule">Epigastric pain </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Muscular pain </td><td align="left" valign="top" styleCode="Botrule Rrule">Excessive thirst </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Breast tenderness </td><td align="left" valign="top" styleCode="Botrule Rrule">Twitching eyelids </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Eye pain </td><td align="left" valign="top" styleCode="Botrule Rrule">Gagging, retching </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Drowsiness </td><td align="left" valign="top" styleCode="Botrule Rrule">Dry throat </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Dystonia </td><td align="left" valign="top" styleCode="Botrule Rrule">Sensation of choking </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Asthma </td><td align="left" valign="top" styleCode="Botrule Rrule">Thyroid storm </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Injection site pain </td><td align="left" valign="top" styleCode="Botrule Rrule">Syncope </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Tinnitus </td><td align="left" valign="top" styleCode="Botrule Rrule">Palpitations </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Vertigo </td><td align="left" valign="top" styleCode="Botrule Rrule">Rash </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Vaso-vagal syndrome </td><td align="left" valign="top" styleCode="Botrule Rrule">Upper respiratory infection </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Dryness of mouth </td><td align="left" valign="top" styleCode="Botrule Rrule">Leg cramps </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Hyperventilation </td><td align="left" valign="top" styleCode="Botrule Rrule">Perforated uterus </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Respiratory distress </td><td align="left" valign="top" styleCode="Botrule Rrule">Anxiety </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Hematemesis </td><td align="left" valign="top" styleCode="Botrule Rrule">Chest pain </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Taste alterations </td><td align="left" valign="top" styleCode="Botrule Rrule">Retained placental fragment </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Urinary tract infection </td><td align="left" valign="top" styleCode="Botrule Rrule">Shortness of breath </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Septic shock </td><td align="left" valign="top" styleCode="Botrule Rrule">Fullness of throat </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Torticollis </td><td align="left" valign="top" styleCode="Botrule Rrule">Uterine sacculation </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Lethargy </td><td align="left" valign="top" styleCode="Botrule Rrule">Faintness, light- headedness </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Hypertension </td><td align="left" valign="top" styleCode="Botrule Rrule">Uterine rupture </td></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Tachycardia </td><td align="left" valign="top" styleCode="Botrule Rrule"/></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Pulmonary edema </td><td align="left" valign="top" styleCode="Botrule Rrule"/></tr><tr><td align="left" valign="top" styleCode="Botrule Lrule Rrule">Endometritis from IUCD </td><td align="left" valign="top" styleCode="Botrule Rrule"/></tr></tbody></table>

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.