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Summary

FDA Adverse Reports: 63. View All

Ultane FDA safety alerts: 2003

Reported deaths: 11

Reported hospitalizations: 4

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Often additional risks of using a medication, such as Ultane, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Ultane users, Learn more about unwanted side effects & find ways to reduce them. Browse Ultane Adverse Reports reported to FDA and participate in Ultane discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Ultane. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Ultane Adverse Effect Reports (FDA)

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6675703-9 | Hyperthermia Malignant
on Apr 01, 2010 Female patient from UNITED STATES , weighting 38.74 lb, was diagnosed with surgery (What is surgery?), tooth repair, dental caries and was treated with Ultane (View Usage). Patient experienced the following unwanted or unexpected effects: hyperthermia malignant. Ultane dosage: . During the same period patient was treated with PROPOFOL (View Propofol Review and Propofol Label ), ANCEF (View Ancef Review and Ancef Label ), FENTANYL 100 (View Fentanyl-100 Review and Fentanyl-100 Label ).

6264239-5 | Premature Recovery From Anaesthesia
Patient was taking Ultane (View Usage). Patient had the following side effects: premature recovery from anaesthesia on Jul 02, 2009 from SOUTH AFRICA Additional patient health information: Male patient , 55 years of age, was diagnosed with haemorrhoid operation, induction of anaesthesia and. Ultane dosage: . During the same period patient was treated with DIPRIVAN (View Diprivan Review and Diprivan Label ), ALFENTANIL (View Alfentanil Review and Alfentanil Label ), MIVACURIUM (View Mivacurium Review and Mivacurium Label ), MIDAZOLAM HCL (View Midazolam Hcl Review and Midazolam Hcl Label ), GRANISETRON HCL (View Granisetron Hcl Review and Granisetron Hcl Label ), KETOROLAC TROMETHAMINE (View Ketorolac Tromethamine Review and Ketorolac Tromethamine Label ), NITROUS OXIDE (View Nitrous Oxide Review and Nitrous Oxide Label ).

6255305-9 | Anaesthetic Complication
Adverse event was reported on Apr 16, 2009 by a Female patient taking Ultane (View Usage) (Dosage: ) was diagnosed with tonsillectomy, adenoidectomy and. Location: UNITED STATES , child 8 years of age, After Ultane was administered, patient had the following side effects: anaesthetic complication.

6255303-5 | Anaesthetic Complication
on Mar 31, 2009 Female patient from UNITED STATES , child 7 years of age, was diagnosed with tonsillectomy, adenoidectomy and was treated with Ultane (View Usage). Patient experienced the following unwanted or unexpected effects: anaesthetic complication. Ultane dosage: .


6255300-X | Anaesthetic Complication
on Mar 31, 2009 Female patient from UNITED STATES , child 10 years of age, was diagnosed with facial bones fracture and was treated with Ultane (View Usage). Patient had the following side effects: anaesthetic complication. Ultane dosage: .

6255285-6 | Anaesthetic Complication
Patient was taking Ultane (View Usage). After Ultane was administered, patient had the following side effects: anaesthetic complication on Apr 16, 2009 from UNITED STATES Additional patient health information: Female patient , child 4 years of age, was diagnosed with myringotomy and. Ultane dosage: .

6255284-4 | Anaesthetic Complication
Adverse event was reported on Mar 31, 2009 by a Female patient taking Ultane (View Usage) (Dosage: ) was diagnosed with tonsillectomy and. Location: UNITED STATES , child 6 years of age, Patient experienced the following unwanted or unexpected effects: anaesthetic complication.

6255283-2 | Anaesthetic Complication
on Mar 31, 2009 Female patient from UNITED STATES , child 5 years of age, was diagnosed with myringotomy, adenoidectomy and was treated with Ultane (View Usage). Patient had the following side effects: anaesthetic complication. Ultane dosage: .

6255282-0 | Anaesthetic Complication
on Apr 16, 2009 Female patient from UNITED STATES , child 6 years of age, was diagnosed with tonsillectomy, adenoidectomy and was treated with Ultane (View Usage). After Ultane was administered, patient had the following side effects: anaesthetic complication. Ultane dosage: .

6255280-7 | Anaesthetic Complication
Patient was taking Ultane (View Usage). Patient experienced the following unwanted or unexpected effects: anaesthetic complication on Apr 16, 2009 from UNITED STATES Additional patient health information: Female patient , child 3 years of age, was diagnosed with tonsillectomy, adenoidectomy and. Ultane dosage: .

6255279-0 | Anaesthetic Complication
Adverse event was reported on Apr 16, 2009 by a Female patient taking Ultane (View Usage) (Dosage: ) was diagnosed with myringotomy, adenoidectomy and. Location: UNITED STATES , child 5 years of age, Patient had the following side effects: anaesthetic complication.

6255277-7 | Anaesthetic Complication
on Apr 16, 2009 Female patient from UNITED STATES , child 3 years of age, was diagnosed with tonsillectomy, adenoidectomy and was treated with Ultane (View Usage). After Ultane was administered, patient had the following side effects: anaesthetic complication. Ultane dosage: .

6255276-5 | Anaesthetic Complication
on Mar 31, 2009 Female patient from UNITED STATES , child 7 years of age, was diagnosed with myringotomy and was treated with Ultane (View Usage). Patient experienced the following unwanted or unexpected effects: anaesthetic complication. Ultane dosage: .

6255275-3 | Anaesthetic Complication
Patient was taking Ultane (View Usage). Patient had the following side effects: anaesthetic complication on Apr 16, 2009 from UNITED STATES Additional patient health information: Female patient , child 11 years of age, was diagnosed with tonsillectomy, adenoidectomy and. Ultane dosage: .

6255274-1 | Anaesthetic Complication
Adverse event was reported on Apr 16, 2009 by a Female patient taking Ultane (View Usage) (Dosage: ) was diagnosed with tonsillectomy, adenoidectomy and. Location: UNITED STATES , child 9 years of age, After Ultane was administered, patient had the following side effects: anaesthetic complication.

6255273-X | Anaesthetic Complication
on Apr 16, 2009 Female patient from UNITED STATES , child 3 years of age, was diagnosed with myringotomy and was treated with Ultane (View Usage). Patient experienced the following unwanted or unexpected effects: anaesthetic complication. Ultane dosage: .

6255272-8 | Anaesthetic Complication
on Apr 16, 2009 Female patient from UNITED STATES , child 9 years of age, was diagnosed with tonsillectomy, adenoidectomy and was treated with Ultane (View Usage). Patient had the following side effects: anaesthetic complication. Ultane dosage: .

6255271-6 | Anaesthetic Complication
Patient was taking Ultane (View Usage). After Ultane was administered, patient had the following side effects: anaesthetic complication on Apr 16, 2009 from UNITED STATES Additional patient health information: Female patient , 13 years of age, was diagnosed with myringotomy and. Ultane dosage: .

6255269-8 | Anaesthetic Complication
Adverse event was reported on Apr 16, 2009 by a Female patient taking Ultane (View Usage) (Dosage: ) was diagnosed with myringotomy, adenoidectomy and. Location: UNITED STATES , child 2 years of age, Patient experienced the following unwanted or unexpected effects: anaesthetic complication.

6255266-2 | Anaesthetic Complication
on Mar 31, 2009 Female patient from UNITED STATES , child 3 years of age, was diagnosed with adenoidectomy and was treated with Ultane (View Usage). Patient had the following side effects: anaesthetic complication. Ultane dosage: .

6255265-0 | Anaesthetic Complication
on Mar 31, 2009 Female patient from UNITED STATES , child 3 years of age, was diagnosed with adenoidectomy and was treated with Ultane (View Usage). After Ultane was administered, patient had the following side effects: anaesthetic complication. Ultane dosage: .

6255264-9 | Anaesthetic Complication
Patient was taking Ultane (View Usage). Patient experienced the following unwanted or unexpected effects: anaesthetic complication on Apr 16, 2009 from UNITED STATES Additional patient health information: Female patient , child 6 years of age, was diagnosed with myringotomy, tonsillectomy, adenoidectomy and. Ultane dosage: .

6255262-5 | Anaesthetic Complication
Adverse event was reported on Apr 16, 2009 by a Female patient taking Ultane (View Usage) (Dosage: ) was diagnosed with myringotomy, adenoidectomy and. Location: UNITED STATES , child 2 years of age, Patient had the following side effects: anaesthetic complication.

6255261-3 | Anaesthetic Complication
on Apr 16, 2009 Female patient from UNITED STATES , child 4 years of age, was diagnosed with tonsillectomy, adenoidectomy and was treated with Ultane (View Usage). After Ultane was administered, patient had the following side effects: anaesthetic complication. Ultane dosage: .

6255260-1 | Anaesthetic Complication
on Apr 16, 2009 Female patient from UNITED STATES , child 7 years of age, was diagnosed with adenoidectomy and was treated with Ultane (View Usage). Patient experienced the following unwanted or unexpected effects: anaesthetic complication. Ultane dosage: .

6255259-5 | Anaesthetic Complication
Patient was taking Ultane (View Usage). Patient had the following side effects: anaesthetic complication on Apr 16, 2009 from UNITED STATES Additional patient health information: Female patient , child 2 years of age, was diagnosed with adenoidectomy and. Ultane dosage: .

6255257-1 | Anaesthetic Complication
Adverse event was reported on Apr 16, 2009 by a Female patient taking Ultane (View Usage) (Dosage: ) was diagnosed with tonsillectomy, adenoidectomy and. Location: UNITED STATES , child 9 years of age, After Ultane was administered, patient had the following side effects: anaesthetic complication.

6255252-2 | Hepatitis Cholestatic
on Sep 17, 2008 Male patient from UNITED STATES , weighting 149.9 lb, was diagnosed with blood pressure (What is blood pressure?), vitamin supplementation and was treated with Ultane (View Usage). Patient experienced the following unwanted or unexpected effects: hepatitis cholestatic. Ultane dosage: Not Reported. During the same period patient was treated with METOPROLOL SUCCINATE (View Metoprolol Succinate Review and Metoprolol Succinate Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ).

6255249-2 | Anaphylactic Reaction, Hypotension, Wheezing
on Mar 18, 2009 Female patient from UNITED STATES , weighting 280.3 lb, was treated with Ultane (View Usage). Patient had the following side effects: anaphylactic reaction, hypotension, wheezing. Ultane dosage: .

6255248-0 | Orthostatic Hypotension, Syncope
Patient was taking Ultane (View Usage). After Ultane was administered, patient had the following side effects: orthostatic hypotension, syncope on Jul 28, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 118.1 lb, . Ultane dosage: .

6219001-6 | Premature Recovery From Anaesthesia
Adverse event was reported on May 29, 2009 by a Male patient taking Ultane (View Usage) (Dosage: ) was diagnosed with haemorrhoid operation, induction of anaesthesia and. Location: SOUTH AFRICA , 55 years of age, Patient experienced the following unwanted or unexpected effects: premature recovery from anaesthesia. During the same period patient was treated with DIPRIVAN (View Diprivan Review and Diprivan Label ), ALFENTANIL (View Alfentanil Review and Alfentanil Label ), MIVACURIUM (View Mivacurium Review and Mivacurium Label ), MIDAZOLAM HCL (View Midazolam Hcl Review and Midazolam Hcl Label ), GRANISETRON HCL (View Granisetron Hcl Review and Granisetron Hcl Label ), KETOROLAC TROMETHAMINE (View Ketorolac Tromethamine Review and Ketorolac Tromethamine Label ), NITROUS OXIDE (View Nitrous Oxide Review and Nitrous Oxide Label ).

5782225-6 | Convulsion
on Apr 24, 2008 Female patient from UNITED STATES , child 4 years of age, was diagnosed with surgery (What is surgery?) and was treated with Ultane (View Usage). Patient had the following side effects: convulsion. Ultane dosage: Mask Induction. During the same period patient was treated with OXYGEN (High Flow) (View Oxygen Review and Oxygen Label ).

5782224-4 | Feeling Abnormal, Headache, Hypertension
on May 02, 2008 Male patient from UNITED STATES , weighting 167.2 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Ultane (View Usage). After Ultane was administered, patient had the following side effects: feeling abnormal, headache (What is headache?), hypertension. Ultane dosage: Vaporizers. During the same period patient was treated with OMEPRAZOLE (40 Mg Daily, As Needed) (View Omeprazole Review and Omeprazole Label ).

5782214-1 | Convulsion
Patient was taking Ultane (View Usage). Patient experienced the following unwanted or unexpected effects: convulsion on Apr 24, 2008 from UNITED STATES Additional patient health information: Male patient , child 6 years of age, was diagnosed with surgery (What is surgery?) and. Ultane dosage: Induction. During the same period patient was treated with OXYGEN (View Oxygen Review and Oxygen Label ).

5705113-X | Arrhythmia
Adverse event was reported on Apr 07, 2008 by a Male patient taking Ultane (View Usage) (Dosage: Not Reported) . Location: UNITED STATES , 47 years of age, weighting 204.2 lb, Patient had the following side effects: arrhythmia (What is arrhythmia?).

5699152-5 | Unwanted Awareness During Anaesthesia
on Apr 04, 2008 Female patient from UNITED STATES , 40 years of age, weighting 196.0 lb, was diagnosed with induction of anaesthesia and was treated with Ultane (View Usage). After Ultane was administered, patient had the following side effects: unwanted awareness during anaesthesia. Ultane dosage: Inhal.

5699139-2 | Unwanted Awareness During Anaesthesia
on Apr 07, 2008 Male patient from UNITED STATES , 37 years of age, weighting 160.1 lb, was diagnosed with induction of anaesthesia and was treated with Ultane (View Usage). Patient experienced the following unwanted or unexpected effects: unwanted awareness during anaesthesia. Ultane dosage: Inhal.

5663298-8 | Acute Hepatic Failure
Patient was taking Ultane (View Usage). Patient had the following side effects: acute hepatic failure on Mar 05, 2008 from UNITED STATES Additional patient health information: Female patient , 25 years of age, was diagnosed with anaesthesia, caesarean section and. Ultane dosage: . Patient was hospitalized.

5536225-1 | Arrhythmia, Cardiomegaly, Contusion, Pulmonary Congestion, Unresponsive To Stimuli
Adverse event was reported on Dec 04, 2007 by a Male patient taking Ultane (View Usage) (Dosage: Not Reported) . Location: UNITED STATES , 47 years of age, weighting 204.2 lb, After Ultane was administered, patient had the following side effects: arrhythmia (What is arrhythmia?), cardiomegaly, contusion, pulmonary congestion, unresponsive to stimuli.

5445890-9 | Convulsion
on Dec 08, 2006 Female patient from UNITED STATES , child 8 years of age, weighting 48.50 lb, was diagnosed with sedation and was treated with Ultane (View Usage). Patient experienced the following unwanted or unexpected effects: convulsion. Ultane dosage: 8 %, Aerosol, Inhalation.

5409981-0 | Hemiplegia, Muscular Weakness, Paresis
on Jul 31, 2007 Female patient from SOUTH AFRICA , 33 years of age, was diagnosed with anaesthesia, analgesia, epilepsy (What is epilepsy?) and was treated with Ultane (View Usage). Patient had the following side effects: hemiplegia, muscular weakness, paresis. Ultane dosage: . During the same period patient was treated with TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ), PROPOFOL (View Propofol Review and Propofol Label ), VECURONIUM BROMIDE (View Vecuronium Bromide Review and Vecuronium Bromide Label ), REMIFENTANIL HYDROCHLORIDE (View Remifentanil Hydrochloride Review and Remifentanil Hydrochloride Label ), OXYGEN (View Oxygen Review and Oxygen Label ).

5394600-2 | Muscular Weakness, Paresis
Patient was taking Ultane (View Usage). After Ultane was administered, patient had the following side effects: muscular weakness, paresis on Jul 13, 2007 from SOUTH AFRICA Additional patient health information: Female patient , 33 years of age, was diagnosed with anaesthesia, analgesia, epilepsy (What is epilepsy?) and. Ultane dosage: . During the same period patient was treated with TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ).

5308776-6 | Muscular Weakness
Adverse event was reported on Apr 16, 2007 by a Female patient taking Ultane (View Usage) (Dosage: ) was diagnosed with anaesthesia, analgesic effect, epilepsy (What is epilepsy?) and. Location: SOUTH AFRICA , 33 years of age, Patient experienced the following unwanted or unexpected effects: muscular weakness. During the same period patient was treated with TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ).

5234345-2 | Respiratory Disorder, Thrombosis, Unevaluable Event
on Feb 01, 2007 Female patient from UNITED STATES , weighting 119.1 lb, was diagnosed with occupational problem environmental, anaesthesia, rhinitis allergic, hysterectomy (What is hysterectomy?) and was treated with Ultane (View Usage). Patient had the following side effects: respiratory disorder, thrombosis, unevaluable event. Ultane dosage: . During the same period patient was treated with CALCIUM (View Calcium Review and Calcium Label ), VITAMINS (View Vitamins Review and Vitamins Label ), ACTIFED (View Actifed Review and Actifed Label ), PSEUDOEPHEDRINE HYDROCHLORIDE (View Pseudoephedrine Hydrochloride Review and Pseudoephedrine Hydrochloride Label ), ESTROGENS CONJUGATED (View Estrogens Conjugated Review and Estrogens Conjugated Label ).

5167620-0 | Hepatic Failure, Hepatocellular Damage, Hypotension, Malaise, Nausea
on Nov 17, 2006 Male patient from SOUTH AFRICA , 59 years of age, was diagnosed with anaesthesia, ischaemic heart disease prophylaxis, blood cholesterol increased, induction of anaesthesia, pain (What is pain?) and was treated with Ultane (View Usage). After Ultane was administered, patient had the following side effects: hepatic failure, hepatocellular damage, hypotension, malaise, nausea (What is nausea?). Ultane dosage: . During the same period patient was treated with ACETYLSALICYLIC ACID SRT (View Acetylsalicylic Acid Srt Review and Acetylsalicylic Acid Srt Label ), ATORVASTATIN CALCIUM (View Atorvastatin Calcium Review and Atorvastatin Calcium Label ), PROPOFOL (View Propofol Review and Propofol Label ), ROCURONIUM BROMIDE (View Rocuronium Bromide Review and Rocuronium Bromide Label ), ONDANSETRON HCL (View Ondansetron Hcl Review and Ondansetron Hcl Label ), REMIFENTANIL HYDROCHLORIDE (View Remifentanil Hydrochloride Review and Remifentanil Hydrochloride Label ), CEFAZOLIN SODIUM (View Cefazolin Sodium Review and Cefazolin Sodium Label ), CYCLIMORPH (View Cyclimorph Review and Cyclimorph Label ).

5072296-7 | Hypertension, Somnolence, Tachycardia
Patient was taking Ultane (View Usage). Patient experienced the following unwanted or unexpected effects: hypertension, somnolence, tachycardia on Oct 17, 2005 from UNITED STATES Additional patient health information: Female patient , child 3 years of age, weighting 39.68 lb, . Ultane dosage: See Image. During the same period patient was treated with PROPOFOL (View Propofol Review and Propofol Label ), LIDOCAINE (View Lidocaine Review and Lidocaine Label ), DEXAMETHASONE (View Dexamethasone Review and Dexamethasone Label ), FENTANYL (View Fentanyl Review and Fentanyl Label ), OXYGEN (View Oxygen Review and Oxygen Label ).

5011733-0 | Anaesthetic Complication, Anaphylactic Shock, Blood Pressure Decreased, Pulse Absent
Adverse event was reported on May 23, 2006 by a Male patient taking Ultane (View Usage) (Dosage: ) was diagnosed with renal failure chronic and. Location: UNITED STATES , 63 years of age, Patient had the following side effects: anaesthetic complication, anaphylactic shock, blood pressure decreased, pulse absent. During the same period patient was treated with SEVOFLUANCE (View Sevofluance Review and Sevofluance Label ), FENTANYL (View Fentanyl Review and Fentanyl Label ), MIDAZOLAM HCL (View Midazolam Hcl Review and Midazolam Hcl Label ), NIMBEX (View Nimbex Review and Nimbex Label ), SUCCINYLCHOLINE (View Succinylcholine Review and Succinylcholine Label ), PROPOFOL (View Propofol Review and Propofol Label ), LIDOCAINE (View Lidocaine Review and Lidocaine Label ). Patient was hospitalized and became disabled.

4983272-4 | Loss Of Consciousness
on Dec 29, 2005 Male patient from UNITED STATES , 38 years of age, was treated with Ultane (View Usage). After Ultane was administered, patient had the following side effects: loss of consciousness. Ultane dosage: .

4980303-2 | Grand Mal Convulsion
on Apr 13, 2006 Male patient from SOUTH AFRICA , child 6 years of age, was diagnosed with induction of anaesthesia and was treated with Ultane (View Usage). Patient experienced the following unwanted or unexpected effects: grand mal convulsion. Ultane dosage: .

4953544-8 | Bronchopneumonia, Cardiac Failure, Coma, Convulsion, Embolism, Sepsis
Patient was taking Ultane (View Usage). Patient had the following side effects: bronchopneumonia, cardiac failure, coma, convulsion, embolism, sepsis (What is sepsis?) on Mar 17, 2006 from UNITED STATES Additional patient health information: Male patient , 40 years of age, was diagnosed with anaesthesia and. Ultane dosage: .

Showing 1-50 of 63  Next Page  >


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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Ultane risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Ultane quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Ultane use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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(View Anectine Review and Anectine Label ), ULTANE (Dose: Unk) (View Ultane Review and Ultane Label ), OXYGEN (Dose: Unk) (View Oxygen Review and Oxygen Label ), ...

ultane Episodes: 1: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: xeloda Episodes: 1: Diagnosed with major depression.Side ...

... Midazolam Label ), FENTANYL (View Fentanyl Review and Fentanyl Label ), PROPOFOL (View Propofol Review and Propofol Label ), ULTANE (View Ultane Review and Ultane Label ).

During the same period patient was treated with FENTANYL (View Fentanyl Review and Fentanyl Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ), ULTANE (1.85 Minimum ...

ulsanic Episodes: 1: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: ultane Episodes: 2: Diagnosed with major depression.Side ...

... 2.5 Mg) (View Propofol Review and Propofol Label ), FENOFIBRATE (Oral) (View Fenofibrate Review and Fenofibrate Label ), ULTANE (View Ultane Review and Ultane Label ), ...

... treated with PROPOFOL (Dose: Unk) (View Propofol Review and Propofol Label ), ANECTINE (Dose: Unk) (View Anectine Review and Anectine Label ), ULTANE (Dose: Unk) (View Ultane ...

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Ultane Reactions
Acute Hepatic Failure
Anaesthetic Complication
Anaphylactic Reaction
Anaphylactic Shock
ArrhythmiaWhat is Arrhythmia?
Blood Pressure Decreased
Bradycardia
Bronchopneumonia
Cardiac ArrestWhat is Cardiac arrest?
Cardiac Failure
Cardiomegaly
Coma
Convulsion
Fluorosis
Haemodialysis
Haemorrhage
Hyperkalaemia
Hypertension
Hyperthermia Malignant
Hypotension
Loss Of Consciousness
Metabolic Acidosis
Multi-organ Failure
Muscular Weakness
Overdose
Paresis
Premature Recovery From Anaesthesia
Rhabdomyolysis
Suicide Attempt
Unwanted Awareness During Anaesthesia
Ultane Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Ultane adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!