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ULTANE Safety Reports
Total ULTANE reports: 8.ULTANE FDA safety alerts: 2003 2007 .
Reported hospitalizations: 1.
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Physician from UNITED STATES reported ULTANE problem on Feb 01, 2007. Female patient, weighting 119.1 lb, was diagnosed with occupational problem environmental, anaesthesia, rhinitis allergic, hysterectomy and was treated with ULTANE. After drug was administered, patient experienced the following problems/side effects: respiratory disorder, thrombosis, unevaluable event. ULTANE dosage: unknown. During the same period patient was treated with CALCIUM, VITAMINS, ACTIFED, PSEUDOEPHEDRINE HYDROCHLORIDE, ESTROGENS CONJUGATED. Patient recovered.
ULTANE problem was reported by a Physician from SOUTH AFRICA on Apr 16, 2007. Female patient, 33 years of age, was diagnosed with anaesthesia, analgesic effect, epilepsy and was treated with ULTANE. After drug was administered, patient experienced the following problems/side effects: muscular weakness. ULTANE dosage: unknown. During the same period patient was treated with TRAMADOL. Patient recovered.
Physician from UNITED STATES reported ULTANE problem on Oct 17, 2005. Female patient, child 3 years of age, weighting 39.68 lb, was treated with ULTANE. After drug was administered, patient experienced the following problems/side effects: hypertension, somnolence, tachycardia. ULTANE dosage: unknown. During the same period patient was treated with PROPOFOL, LIDOCAINE, DEXAMETHASONE, FENTANYL, OXYGEN. Patient recovered.
ULTANE problem was reported by a Physician from UNITED STATES on Apr 21, 2006. Female patient was diagnosed with anaesthesia and was treated with ULTANE. After drug was administered, patient experienced the following problems/side effects: hepatitis, jaundice, liver function test abnormal. ULTANE dosage: unknown. Patient was hospitalized. Patient recovered.
Physician from SOUTH AFRICA reported ULTANE problem on Nov 17, 2006. Male patient, 59 years of age, was diagnosed with anaesthesia, ischaemic heart disease prophylaxis, blood cholesterol increased, induction of anaesthesia, pain and was treated with ULTANE. After drug was administered, patient experienced the following problems/side effects: hepatic failure, hepatocellular damage, hypotension, malaise, nausea. ULTANE dosage: unknown. During the same period patient was treated with ACETYLSALICYLIC ACID SRT, ATORVASTATIN CALCIUM, PROPOFOL, ROCURONIUM BROMIDE, ONDANSETRON, REMIFENTANIL HYDROCHLORIDE, CEFAZOLIN, CYCLIMORPH. Patient recovered.
ULTANE problem was reported by a Physician from SOUTH AFRICA on July 13, 2007. Female patient, 33 years of age, was diagnosed with anaesthesia, analgesia, epilepsy and was treated with ULTANE. After drug was administered, patient experienced the following problems/side effects: muscular weakness, paresis. ULTANE dosage: unknown. During the same period patient was treated with TRAMADOL. Patient recovered.
Physician from UNITED STATES reported ULTANE problem on Dec 08, 2006. Female patient, child 8 years of age, weighting 48.50 lb, was diagnosed with sedation and was treated with ULTANE. After drug was administered, patient experienced the following problems/side effects: convulsion. ULTANE dosage: unknown. Patient recovered.
ULTANE problem was reported by a Physician from SOUTH AFRICA on July 31, 2007. Female patient, 33 years of age, was diagnosed with anaesthesia, analgesia, epilepsy and was treated with ULTANE. After drug was administered, patient experienced the following problems/side effects: hemiplegia, muscular weakness, paresis. ULTANE dosage: unknown. During the same period patient was treated with TRAMADOL, PROPOFOL, VECURONIUM BROMIDE, REMIFENTANIL HYDROCHLORIDE, OXYGEN. Patient recovered.