PROPOFOL Side Effects

7024772-5 | Hepatitis Acute
on Sep 16, 2010 Female patient from GERMANY , 23 years of age, was diagnosed with oesophagogastroduodenoscopy and was treated with Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: hepatitis acute. Propofol dosage: 480 Mg (cumulative Dose). During the same period patient was treated with IMERON 400 MCT (IOMEPROL) (View Imeron 400 Mct (iomeprol) Review and Imeron 400 Mct (iomeprol) Label ), BUSCOPAN (View Buscopan Review and Buscopan Label ), DORMICUM (NITRAZEPAM) (View Dormicum (nitrazepam) Review and Dormicum (nitrazepam) Label ). Patient was hospitalized.

7020356-3 | Anaphylactic Shock, Face Oedema, Rash, Type I Hypersensitivity
Patient was taking Propofol (View Usage). Patient had the following side effects: anaphylactic shock, face oedema, rash (What is rash?), type i hypersensitivity on Sep 13, 2010 from SWITZERLAND Additional patient health information: Male patient , 33 years of age, . Propofol dosage: . During the same period patient was treated with ACUPAN (View Acupan Review and Acupan Label ), DROPERIDOL (View Droperidol Review and Droperidol Label ), KETALAR (View Ketalar Review and Ketalar Label ), PERFALGAN (PARACETAMOL) (View Perfalgan (paracetamol) Review and Perfalgan (paracetamol) Label ), RAPIDOCAINE (LIDOCAINE HYDROCHLORIDE) (View Rapidocaine (lidocaine Hydrochloride) Review and Rapidocaine (lidocaine Hydrochloride) Label ), ULTIVA (View Ultiva Review and Ultiva Label ), VOLTAREN (View Voltaren Review and Voltaren Label ). Patient was hospitalized.

7020352-6 | Blister, Necrosis, Rash Erythematous
Adverse event was reported on Sep 14, 2010 by a Female patient taking Propofol (View Usage) (Dosage: ) . Location: NORWAY , 60 years of age, After Propofol was administered, patient had the following side effects: blister, necrosis, rash erythematous. During the same period patient was treated with FENTANYL CITRATE(FENTANYL CITRATE) (FENTANYL CITRATE) (View Fentanyl Citrate(fentanyl Citrate) (fentanyl Citrate) Review and Fentanyl Citrate(fentanyl Citrate) (fentanyl Citrate) Label ), ESOMEPRAZOLE (ESOMEPRAZOLE) (ESOMEPRAZOLE) (View Esomeprazole (esomeprazole) (esomeprazole) Review and Esomeprazole (esomeprazole) (esomeprazole) Label ), ISOTONIC SODIUM CHLORIDE (SODIUM CHLORIDE) (SODIUM CHLORIDE) (View Isotonic Sodium Chloride (sodium Chloride) (sodium Chloride) Review and Isotonic Sodium Chloride (sodium Chloride) (sodium Chloride) Label ), TERLIPRESSIN (TERLIPRESSIN) (TERLIPRESSIN) (View Terlipressin (terlipressin) (terlipressin) Review and Terlipressin (terlipressin) (terlipressin) Label ), PROMETHOMPLEX S TIM(PROTHROMPLEX S TIM) (PROTHROMPLEX S TIM) (View Promethomplex S-tim(prothromplex S-tim) (prothromplex S-tim) Review and Promethomplex S-tim(prothromplex S-tim) (prothromplex S-tim) Label ), CALCIUM CHLORIDE DIHYDRATE (CALCIUM CHRLODIE DIHYDRATE) (CALCIUM CHLOR (View Calcium Chloride Dihydrate (calcium Chrlodie Dihydrate) (calcium Chlor Review and Calcium Chloride Dihydrate (calcium Chrlodie Dihydrate) (calcium Chlor Label ), EPHEDRINE (EPHEDRINE) (EPHEDRINE) (View Ephedrine (ephedrine) (ephedrine) Review and Ephedrine (ephedrine) (ephedrine) Label ), BRICANTYL (TERBUTALINE SULFATE) (TERBUTALINE SULFATE) (View Bricantyl (terbutaline Sulfate) (terbutaline Sulfate) Review and Bricantyl (terbutaline Sulfate) (terbutaline Sulfate) Label ).

7018065-X | Electrocardiogram Qt Prolonged, Ventricular Fibrillation
on Sep 20, 2010 Male patient from GERMANY , 55 years of age, weighting 165.3 lb, was diagnosed with anaesthesia and was treated with Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: electrocardiogram qt prolonged, ventricular fibrillation. Propofol dosage: . Patient was hospitalized.


7018040-5 | Anaphylactic Shock, Face Oedema, Hypotension, Oxygen Saturation Decreased, Rash, Type I Hypersensitivity
on Sep 13, 2010 Male patient from GERMANY , 33 years of age, was treated with Propofol (View Usage). Patient had the following side effects: anaphylactic shock, face oedema, hypotension, oxygen saturation decreased, rash (What is rash?), type i hypersensitivity. Propofol dosage: . During the same period patient was treated with ACUPAN (10 Milligram) (View Acupan Review and Acupan Label ), DROPERIDOL (View Droperidol Review and Droperidol Label ), KETALAR (View Ketalar Review and Ketalar Label ), PERFALGAN (View Perfalgan Review and Perfalgan Label ), RAPIDOCAINE (View Rapidocaine Review and Rapidocaine Label ), ULTIVA (View Ultiva Review and Ultiva Label ), VOLTAREN (View Voltaren Review and Voltaren Label ). Patient was hospitalized.

7015481-7 | Anaphylactic Shock
Patient was taking Propofol (View Usage). After Propofol was administered, patient had the following side effects: anaphylactic shock on Sep 21, 2010 from SWITZERLAND Additional patient health information: Female patient , weighting 143.3 lb, was diagnosed with gastric operation and. Propofol dosage: .

6980147-6 | Grand Mal Convulsion
Adverse event was reported on Sep 07, 2010 by a Male patient taking Propofol (View Usage) (Dosage: ) . Location: JAPAN , 23 years of age, Patient experienced the following unwanted or unexpected effects: grand mal convulsion. During the same period patient was treated with MIDAZOLAM HCL (View Midazolam Hcl Review and Midazolam Hcl Label ).

6979381-0 | Chills, Pain, Product Contamination, Pyrexia
on Sep 10, 2010 Female patient from UNITED STATES , 69 years of age, weighting 219.0 lb, was diagnosed with colonoscopy (What is colonoscopy?) and was treated with Propofol (View Usage). Patient had the following side effects: chills, pain (What is pain?), product contamination, pyrexia. Propofol dosage: .

6976027-2 | Bradyarrhythmia, Cardiac Arrest, Heart Injury, Propofol Infusion Syndrome
on Sep 06, 2010 Male patient from TAIWAN, PROVINCE OF CHINA , 24 years of age, was diagnosed with sedation and was treated with Propofol (View Usage). After Propofol was administered, patient had the following side effects: bradyarrhythmia, cardiac arrest (What is cardiac arrest?), heart injury, propofol infusion syndrome. Propofol dosage: 3.0-5.8 Mg/kg/hr.

6965602-7 | Electrocardiogram Qt Prolonged, Torsade De Pointes
Patient was taking Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: electrocardiogram qt prolonged, torsade de pointes on Aug 23, 2010 from JAPAN Additional patient health information: Male patient , 70 years of age, was diagnosed with induction and maintenance of anaesthesia and. Propofol dosage: .

6957002-0 | Chills, Nausea, Pyrexia
Adverse event was reported on Aug 27, 2010 by a Male patient taking Propofol (View Usage) (Dosage: ) . Location: UNITED STATES , 50 years of age, weighting 170.0 lb, Patient had the following side effects: chills, nausea (What is nausea?), pyrexia. During the same period patient was treated with DIPRIVAN (View Diprivan Review and Diprivan Label ).

6956998-0 | Chills, Fatigue, Product Quality Issue, Pyrexia
on Aug 27, 2010 Female patient from UNITED STATES , 55 years of age, weighting 109.0 lb, was treated with Propofol (View Usage). After Propofol was administered, patient had the following side effects: chills, fatigue, product quality issue, pyrexia. Propofol dosage: . During the same period patient was treated with DIPRIVAN (View Diprivan Review and Diprivan Label ).

6956993-1 | Chills, Pyrexia
on Aug 27, 2010 Male patient from UNITED STATES , 47 years of age, weighting 150.0 lb, was treated with Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: chills, pyrexia. Propofol dosage: . During the same period patient was treated with DIPRIVAN (View Diprivan Review and Diprivan Label ).

6956204-7 | Oedema Peripheral, Pulmonary Embolism
Patient was taking Propofol (View Usage). Patient had the following side effects: oedema peripheral, pulmonary embolism (What is pulmonary embolism?) on May 14, 2010 from NORWAY Additional patient health information: Female patient , 75 years of age, was diagnosed with induction of anaesthesia and. Propofol dosage: 120 Mg. During the same period patient was treated with CURACIT (SUXAMETHONIUM CHLORIDE) (SUXAMETHONIUM CHLORIDE) (View Curacit (suxamethonium Chloride) (suxamethonium Chloride) Review and Curacit (suxamethonium Chloride) (suxamethonium Chloride) Label ), APODORM (NITRAZEPAM) (NITRAZEPAM) (View Apodorm (nitrazepam) (nitrazepam) Review and Apodorm (nitrazepam) (nitrazepam) Label ), FLUTIDE (FLUTICASONE PROPIONATE) (FLUTICASONE PROPIONATE) (View Flutide (fluticasone Propionate) (fluticasone Propionate) Review and Flutide (fluticasone Propionate) (fluticasone Propionate) Label ), SINEMET 25/100 (SINEMET) (SINEMET) (View Sinemet 25/100 (sinemet) (sinemet) Review and Sinemet 25/100 (sinemet) (sinemet) Label ), SOBRIL (OXAZEPAM) (OXAZEPAM) (View Sobril (oxazepam) (oxazepam) Review and Sobril (oxazepam) (oxazepam) Label ), EDRONAX (REBOXETINE) (REBOXETINE) (View Edronax (reboxetine) (reboxetine) Review and Edronax (reboxetine) (reboxetine) Label ), NORITREN (NORTRIPTYLINE HYDROCHLORIDE) (NORTRIPTYLINE HYDROCHLORIDE) (View Noritren (nortriptyline Hydrochloride) (nortriptyline Hydrochloride) Review and Noritren (nortriptyline Hydrochloride) (nortriptyline Hydrochloride) Label ), SINEMET 12.5/50 (SINEMET) (SINEMET) (View Sinemet 12.5/50 (sinemet) (sinemet) Review and Sinemet 12.5/50 (sinemet) (sinemet) Label ). Patient was hospitalized.

6944848-8 | Electrocardiogram Qt Prolonged, Torsade De Pointes
Adverse event was reported on Aug 23, 2010 by a Male patient taking Propofol (View Usage) (Dosage: ) was diagnosed with induction and maintenance of anaesthesia and. Location: JAPAN , 70 years of age, After Propofol was administered, patient had the following side effects: electrocardiogram qt prolonged, torsade de pointes.

6933655-8 | Trismus
on Aug 03, 2010 Female patient from GERMANY , 54 years of age, was diagnosed with induction of anaesthesia, induction and maintenance of anaesthesia and was treated with Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: trismus. Propofol dosage: 150 Mg, Intravenous Bolus. During the same period patient was treated with CLOMIPRAMINE (CLOMIPRAMINE) (CLOMIPRAMINE) (View Clomipramine (clomipramine) (clomipramine) Review and Clomipramine (clomipramine) (clomipramine) Label ).

6932052-9 | Cardio-respiratory Arrest, Loss Of Consciousness
on Aug 16, 2010 Female patient from CHINA , 45 years of age, weighting 132.3 lb, was diagnosed with anaesthesia and was treated with Propofol (View Usage). Patient had the following side effects: cardio-respiratory arrest, loss of consciousness. Propofol dosage: . During the same period patient was treated with FENTANYL (View Fentanyl Review and Fentanyl Label ), MIDAZOLAM HCL (View Midazolam Hcl Review and Midazolam Hcl Label ), VECURONIUM BROMIDE (View Vecuronium Bromide Review and Vecuronium Bromide Label ).

6930018-6 | Type I Hypersensitivity, Ventricular Extrasystoles
Patient was taking Propofol (View Usage). After Propofol was administered, patient had the following side effects: type i hypersensitivity, ventricular extrasystoles on Aug 13, 2010 from CHINA Additional patient health information: Male patient , 54 years of age, was diagnosed with induction of anaesthesia and. Propofol dosage: Through A Target Controlled Pump. During the same period patient was treated with ATROPINE (View Atropine Review and Atropine Label ), PHENOBARBITAL SODIUM 100MG CAP (View Phenobarbital Sodium 100mg Cap Review and Phenobarbital Sodium 100mg Cap Label ).

6929186-1 | Hepatitis Acute
Adverse event was reported on Jul 28, 2010 by a Female patient taking Propofol (View Usage) (Dosage: 480 Mg (cumulative Dose) Intravenous (not Otherwise Specifed)) . Location: GERMANY , 23 years of age, Patient experienced the following unwanted or unexpected effects: hepatitis acute. Patient was hospitalized.

6925009-5 | Cardio-respiratory Arrest, Loss Of Consciousness
on Aug 10, 2010 Female patient from CHINA , 45 years of age, was diagnosed with anaesthesia and was treated with Propofol (View Usage). Patient had the following side effects: cardio-respiratory arrest, loss of consciousness. Propofol dosage: . During the same period patient was treated with FENTANYL CITRATE (View Fentanyl Citrate Review and Fentanyl Citrate Label ), MIDAZOLAM HCL (View Midazolam Hcl Review and Midazolam Hcl Label ), VECURONIUM BROMIDE (View Vecuronium Bromide Review and Vecuronium Bromide Label ), ISOFLURANE (1-2 Percent) (View Isoflurane Review and Isoflurane Label ), COMPOUND SODIUM LACTATE (View Compound Sodium Lactate Review and Compound Sodium Lactate Label ).

6924996-9 | Hypersensitivity, Ventricular Extrasystoles
on Aug 06, 2010 Male patient from CHINA , 54 years of age, was diagnosed with induction of anaesthesia and was treated with Propofol (View Usage). After Propofol was administered, patient had the following side effects: hypersensitivity, ventricular extrasystoles. Propofol dosage: . During the same period patient was treated with ATROPINE (View Atropine Review and Atropine Label ), PHENOBARBITAL (View Phenobarbital Review and Phenobarbital Label ).

6922773-6 | Asthenia, Dizziness, Type I Hypersensitivity
Patient was taking Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: asthenia, dizziness (What is dizziness?), type i hypersensitivity on Aug 06, 2010 from CHINA Additional patient health information: Female patient , 28 years of age, . Propofol dosage: . During the same period patient was treated with BUTORPHANOL TARTRATE (View Butorphanol Tartrate Review and Butorphanol Tartrate Label ).

6918495-8 | Blood Pressure Increased, Chest Pain, Loss Of Consciousness, Pupillary Reflex Impaired, Respiratory Arrest
Adverse event was reported on Aug 06, 2010 by a Female patient taking Propofol (View Usage) (Dosage: ) was diagnosed with induction of anaesthesia and. Location: UNITED STATES , 85 years of age, Patient had the following side effects: blood pressure increased, chest pain (What is chest pain?), loss of consciousness, pupillary reflex impaired, respiratory arrest. During the same period patient was treated with REMIFENTANIL (View Remifentanil Review and Remifentanil Label ), BUPIVACAINE HCL (View Bupivacaine Hcl Review and Bupivacaine Hcl Label ), XYLOCAINE (View Xylocaine Review and Xylocaine Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), LEVOTHYROXINE (View Levothyroxine Review and Levothyroxine Label ), CARVEDILOL (View Carvedilol Review and Carvedilol Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ). Patient was hospitalized.

6917498-7 | Blood Pressure Increased, Chest Pain, Loss Of Consciousness, Oxygen Saturation Decreased, Pupillary Reflex Impaired, Respiratory Arrest
on Jul 16, 2010 Female patient from SWITZERLAND , 85 years of age, was diagnosed with induction of anaesthesia and was treated with Propofol (View Usage). After Propofol was administered, patient had the following side effects: blood pressure increased, chest pain (What is chest pain?), loss of consciousness, oxygen saturation decreased, pupillary reflex impaired, respiratory arrest. Propofol dosage: 20 Mg, Intravenous. During the same period patient was treated with REMIFENTANIL (REMIFENTANIL) (REMIFENTANIL) (View Remifentanil (remifentanil) (remifentanil) Review and Remifentanil (remifentanil) (remifentanil) Label ), BUPIVACAINE (BUPIVACAINE) (BUPIVACAINE) (View Bupivacaine (bupivacaine) (bupivacaine) Review and Bupivacaine (bupivacaine) (bupivacaine) Label ), XYLOCAINE (LIDOCAINE) (LIDOCAINE) (View Xylocaine (lidocaine) (lidocaine) Review and Xylocaine (lidocaine) (lidocaine) Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), LEVOTHYROXINE (LEVOTHYROXINE) (LEVOTHYROXINE) (View Levothyroxine (levothyroxine) (levothyroxine) Review and Levothyroxine (levothyroxine) (levothyroxine) Label ), CARVEDILOL (CARVEDILOL) (CVARVEDILOL) (View Carvedilol (carvedilol) (cvarvedilol) Review and Carvedilol (carvedilol) (cvarvedilol) Label ), OMEPRAZOL (OMEPRAZOLE) (OMEPRAZOLE) (View Omeprazol (omeprazole) (omeprazole) Review and Omeprazol (omeprazole) (omeprazole) Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ). Patient was hospitalized.

6910543-4 | Blood Pressure Increased, Chest Pain, Loss Of Consciousness, Pupillary Reflex Impaired, Respiratory Arrest
on Jul 28, 2010 Female patient from UNITED STATES , 85 years of age, was diagnosed with induction of anaesthesia and was treated with Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure increased, chest pain (What is chest pain?), loss of consciousness, pupillary reflex impaired, respiratory arrest. Propofol dosage: . During the same period patient was treated with REMIFENTANIL (View Remifentanil Review and Remifentanil Label ), BUPIVACAINE HCL (View Bupivacaine Hcl Review and Bupivacaine Hcl Label ), XYLOCAINE (View Xylocaine Review and Xylocaine Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), LEVOTHYROXINE (View Levothyroxine Review and Levothyroxine Label ), CARVEDILOL (View Carvedilol Review and Carvedilol Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ). Patient was hospitalized.

6910476-3 | Grand Mal Convulsion, Stress Cardiomyopathy
Patient was taking Propofol (View Usage). Patient had the following side effects: grand mal convulsion, stress cardiomyopathy on Jul 30, 2010 from KOREA, REPUBLIC OF Additional patient health information: Female patient , 67 years of age, weighting 158.7 lb, was diagnosed with induction of anaesthesia, maintenance of anaesthesia and. Propofol dosage: . During the same period patient was treated with SEVOFLURANE (View Sevoflurane Review and Sevoflurane Label ), REMIFENTANIL (2 Mg/kg) (View Remifentanil Review and Remifentanil Label ), MIDAZOLAM HCL (View Midazolam Hcl Review and Midazolam Hcl Label ), GLYCOPYRROLATE (View Glycopyrrolate Review and Glycopyrrolate Label ), ROCURONIUM BROMIDE (View Rocuronium Bromide Review and Rocuronium Bromide Label ).

6907708-4 | Respiratory Depression, Somatoform Disorder Neurologic
Adverse event was reported on Jul 28, 2010 by a Female patient taking Propofol (View Usage) (Dosage: ) was diagnosed with abortion induced and. Location: CHINA , 24 years of age, weighting 101.4 lb, After Propofol was administered, patient had the following side effects: respiratory depression, somatoform disorder neurologic.

6907694-7 | Somatoform Disorder Neurologic
on Jul 28, 2010 Female patient from CHINA , 26 years of age, weighting 121.3 lb, was diagnosed with abortion induced and was treated with Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: somatoform disorder neurologic. Propofol dosage: .

6907659-5 | Hepatitis Acute
on Jul 27, 2010 Female patient from GERMANY , 23 years of age, weighting 149.9 lb, was treated with Propofol (View Usage). Patient had the following side effects: hepatitis acute. Propofol dosage: . Patient was hospitalized.

6896844-7 | Agitation, Blood Creatine Phosphokinase Increased, Brugada Syndrome, Circulatory Collapse, Condition Aggravated, Electrocardiogram Change, Hyperkalaemia, Hypotension
Patient was taking Propofol (View Usage). After Propofol was administered, patient had the following side effects: agitation, blood creatine phosphokinase increased, brugada syndrome, circulatory collapse, condition aggravated, electrocardiogram change, hyperkalaemia, hypotension on Jul 12, 2010 from CANADA Additional patient health information: Male patient , 22 years of age, was diagnosed with sedation and. Propofol dosage: (90 - 100 Mcg/kg/min) Intravenous (not Otherwise Specified). During the same period patient was treated with FENTANYL (View Fentanyl Review and Fentanyl Label ). Patient was hospitalized.

6894764-5 | Cardiac Arrest, Haemorrhage
Adverse event was reported on Jul 30, 2010 by a Male patient taking Propofol (View Usage) (Dosage: ) . Location: UNITED STATES , weighting 200.0 lb, Patient experienced the following unwanted or unexpected effects: cardiac arrest (What is cardiac arrest?), haemorrhage.

6882495-7 | Circulatory Collapse
on Jul 20, 2010 Male patient from DENMARK , 36 years of age, weighting 231.5 lb, was diagnosed with induction of anaesthesia and was treated with Propofol (View Usage). Patient had the following side effects: circulatory collapse. Propofol dosage: 200 Mg. During the same period patient was treated with REMIFENTANIL (40 Microgram) (View Remifentanil Review and Remifentanil Label ), SUXAMETHONIUM (150 Mg) (View Suxamethonium Review and Suxamethonium Label ), TRENBOLONE (Every Other Day) (View Trenbolone Review and Trenbolone Label ), TESTOSTERONENANTAT (Every Other Day) (View Testosteronenantat Review and Testosteronenantat Label ), GROWTH HORMONE (Every Other Day) (View Growth Hormone Review and Growth Hormone Label ), INSULIN (Every Other Day) (View Insulin Review and Insulin Label ), HYDROCORTISONSUCCINATE (100 Mg) (View Hydrocortisonsuccinate Review and Hydrocortisonsuccinate Label ), LIDOCAINE W/ EPINEPHRINE (3 Ml 20 Mg And 5 Microgram/ml) (View Lidocaine W/ Epinephrine Review and Lidocaine W/ Epinephrine Label ).

6882370-8 | Anaphylactic Reaction
on Jul 28, 2010 Male patient from UNITED STATES , 59 years of age, was treated with Propofol (View Usage). After Propofol was administered, patient had the following side effects: anaphylactic reaction. Propofol dosage: 200 Mg Once Iv. During the same period patient was treated with LIDOCAINE (Once Top) (View Lidocaine Review and Lidocaine Label ). Patient was hospitalized.

6882162-X | Pancreatitis Acute
Patient was taking Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: pancreatitis acute on Jul 20, 2010 from GERMANY Additional patient health information: Female patient , 73 years of age, weighting 154.3 lb, was diagnosed with uterine cervical erosion, induction of anaesthesia, postoperative analgesia and. Propofol dosage: . During the same period patient was treated with SUFENTANIL (View Sufentanil Review and Sufentanil Label ), BERLOSIN (View Berlosin Review and Berlosin Label ).

6882001-7 | Pancreatitis Acute
Adverse event was reported on Jul 20, 2010 by a Female patient taking Propofol (View Usage) (Dosage: ) was diagnosed with induction of anaesthesia and. Location: GERMANY , 67 years of age, weighting 187.4 lb, Patient had the following side effects: pancreatitis acute. Patient was hospitalized.

6881995-3 | Dystonia, Unwanted Awareness During Anaesthesia
on Jul 20, 2010 Female patient from UNITED KINGDOM , 85 years of age, was diagnosed with sedation, induction of anaesthesia and was treated with Propofol (View Usage). After Propofol was administered, patient had the following side effects: dystonia (What is dystonia?), unwanted awareness during anaesthesia. Propofol dosage: .

6878005-0 | Blood Pressure Increased, Chest Pain, Loss Of Consciousness, Pupillary Reflex Impaired, Respiratory Arrest
on Jul 16, 2010 Female patient from UNITED STATES , 85 years of age, was diagnosed with induction of anaesthesia and was treated with Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure increased, chest pain (What is chest pain?), loss of consciousness, pupillary reflex impaired, respiratory arrest. Propofol dosage: . During the same period patient was treated with REMIFENTANIL (View Remifentanil Review and Remifentanil Label ), BUPIVACAINE HCL (View Bupivacaine Hcl Review and Bupivacaine Hcl Label ), XYLOCAINE (View Xylocaine Review and Xylocaine Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), LEVOTHYROXINE (View Levothyroxine Review and Levothyroxine Label ), CARVEDILOL (View Carvedilol Review and Carvedilol Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ). Patient was hospitalized.

6877007-8 | Cardiogenic Shock
Patient was taking Propofol (View Usage). Patient had the following side effects: cardiogenic shock on Jul 16, 2010 from JAPAN Additional patient health information: Female patient , 39 years of age, weighting 92.59 lb, was diagnosed with induction of anaesthesia, maintenance of anaesthesia and. Propofol dosage: . During the same period patient was treated with SEVOFLURANE (7%) (View Sevoflurane Review and Sevoflurane Label ), NITROUS OXIDE_OXYGEN (40%) (View Nitrous Oxide_oxygen Review and Nitrous Oxide_oxygen Label ), METHOXAMINE HYDROCHLORIDE (1mg-17) (View Methoxamine Hydrochloride Review and Methoxamine Hydrochloride Label ).

6877004-2 | Torsade De Pointes
Adverse event was reported on Jul 20, 2010 by a Female patient taking Propofol (View Usage) (Dosage: ) . Location: AUSTRALIA , 79 years of age, After Propofol was administered, patient had the following side effects: torsade de pointes. During the same period patient was treated with FENTANYL (View Fentanyl Review and Fentanyl Label ), MIDAZOLAM HCL (View Midazolam Hcl Review and Midazolam Hcl Label ), SEVOFLURANE (View Sevoflurane Review and Sevoflurane Label ), VECURONIUM BROMIDE (View Vecuronium Bromide Review and Vecuronium Bromide Label ), GLICLAZIDE (View Gliclazide Review and Gliclazide Label ), INSULIN HUMAN NOS (View Insulin Human Nos Review and Insulin Human Nos Label ), ISOSORBIDE DINITRATE (View Isosorbide Dinitrate Review and Isosorbide Dinitrate Label ), METFORMIN HYDROCHLORIDE (View Metformin Hydrochloride Review and Metformin Hydrochloride Label ).

6876950-3 | Cardiac Arrest, Sinus Bradycardia
on Jul 20, 2010 Male patient from ITALY , 14 years of age, was diagnosed with induction of anaesthesia and was treated with Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: cardiac arrest (What is cardiac arrest?), sinus bradycardia. Propofol dosage: . During the same period patient was treated with ATRACURIUM BESYLATE (View Atracurium Besylate Review and Atracurium Besylate Label ).

6876949-7 | Blood Creatine Phosphokinase Increased, Rhabdomyolysis
on Jul 21, 2010 Female patient from GERMANY , 14 years of age, weighting 105.8 lb, was diagnosed with anaesthesia and was treated with Propofol (View Usage). Patient had the following side effects: blood creatine phosphokinase increased, rhabdomyolysis. Propofol dosage: . During the same period patient was treated with SUCCINYLCHOLIN (View Succinylcholin Review and Succinylcholin Label ).

6867530-4 | Collapse Of Lung, Product Quality Issue
Patient was taking Propofol (View Usage). After Propofol was administered, patient had the following side effects: collapse of lung, product quality issue on Jul 22, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 185.4 lb, was diagnosed with anaesthesia and. Propofol dosage: See Surgery Notes.

6866185-2 | Dystonia, Unwanted Awareness During Anaesthesia
Adverse event was reported on Jul 13, 2010 by a Female patient taking Propofol (View Usage) (Dosage: ) was diagnosed with sedation and. Location: UNITED KINGDOM , 85 years of age, Patient experienced the following unwanted or unexpected effects: dystonia (What is dystonia?), unwanted awareness during anaesthesia.

6866115-3 | Pancreatitis Acute
on Jul 14, 2010 Female patient from GERMANY , 67 years of age, weighting 187.4 lb, was treated with Propofol (View Usage). Patient had the following side effects: pancreatitis acute. Propofol dosage: . Patient was hospitalized.

6865042-5 | Ischaemia, Penile Vascular Disorder, Procedural Complication
on Jul 05, 2010 Male patient from UNITED KINGDOM , child 4 years of age, was diagnosed with induction of anaesthesia and was treated with Propofol (View Usage). After Propofol was administered, patient had the following side effects: ischaemia, penile vascular disorder, procedural complication. Propofol dosage: (4 Mg/kg). During the same period patient was treated with ATRACURIUM (ATRACURIUM) (ATRACURIUM) (View Atracurium (atracurium) (atracurium) Review and Atracurium (atracurium) (atracurium) Label ), LEVOBUPIVACAINE (LEVOBUPIVACAINE) (LEVOBUPIVACAINE) (View Levobupivacaine (levobupivacaine) (levobupivacaine) Review and Levobupivacaine (levobupivacaine) (levobupivacaine) Label ), CLONIDINE (View Clonidine Review and Clonidine Label ), SEVOFLURANE (SEVOFLURANE) (SEVOFLURANE) (View Sevoflurane (sevoflurane) (sevoflurane) Review and Sevoflurane (sevoflurane) (sevoflurane) Label ), PARACETAMOL (PARACETAMOL) (PARACETAMOL) (View Paracetamol (paracetamol) (paracetamol) Review and Paracetamol (paracetamol) (paracetamol) Label ).

6862469-2 | Haematuria, Lymphopenia, Renal Failure Acute
Patient was taking Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: haematuria, lymphopenia, renal failure acute on Jun 30, 2010 from FRANCE Additional patient health information: Female patient , 40 years of age, was diagnosed with induction of anaesthesia and. Propofol dosage: Intravenous. During the same period patient was treated with ATRACURIUM (View Atracurium Review and Atracurium Label ), ULTIVA (View Ultiva Review and Ultiva Label ), NORMACOL LAVENT ADULTS (BACTRIM) (View Normacol Lavent Adults (bactrim) Review and Normacol Lavent Adults (bactrim) Label ), BETADINE (View Betadine Review and Betadine Label ), BETADINE DERIQUE (POVIDONE IODINE) (View Betadine Derique (povidone-iodine) Review and Betadine Derique (povidone-iodine) Label ), AUGMENTIN '125' (View Augmentin '125' Review and Augmentin '125' Label ), NEURONTINE (GABAPENTIN) (View Neurontine (gabapentin) Review and Neurontine (gabapentin) Label ), KETAMINE PANPHARMA (KETAMINE HYDROCHLORIDE) (View Ketamine Panpharma (ketamine Hydrochloride) Review and Ketamine Panpharma (ketamine Hydrochloride) Label ). Patient was hospitalized.

6862466-7 | Haematuria, Haemolysis, Lymphopenia, Oliguria, Post Procedural Complication, Renal Failure Acute
Adverse event was reported on Jun 30, 2010 by a Female patient taking Propofol (View Usage) (Dosage: Intravenous (not Otherwise Specified)) was diagnosed with induction of anaesthesia and. Location: FRANCE , 46 years of age, Patient had the following side effects: haematuria, haemolysis, lymphopenia, oliguria, post procedural complication, renal failure acute. During the same period patient was treated with ATRACURIUM (View Atracurium Review and Atracurium Label ), SUFENTA PRESERVATIVE FREE (View Sufenta Preservative Free Review and Sufenta Preservative Free Label ), NORMACOL (BACTRIM) (View Normacol (bactrim) Review and Normacol (bactrim) Label ), DROPERIDOL (View Droperidol Review and Droperidol Label ), AUGMENTIN '125' (View Augmentin '125' Review and Augmentin '125' Label ), SEVOFLURANE (View Sevoflurane Review and Sevoflurane Label ), KALINOX (ENTONOX) (View Kalinox (entonox) Review and Kalinox (entonox) Label ). Patient was hospitalized.

6862457-6 | Haematuria, Renal Failure Acute
on Jun 30, 2010 Female patient from FRANCE , 49 years of age, was diagnosed with induction of anaesthesia and was treated with Propofol (View Usage). After Propofol was administered, patient had the following side effects: haematuria, renal failure acute. Propofol dosage: Intravenous (not Otherwise Specified). During the same period patient was treated with ATRACURIUM HOSPIRA (ATRACURIUM) (View Atracurium Hospira (atracurium) Review and Atracurium Hospira (atracurium) Label ), SUFENTA PRESERVATIVE FREE (View Sufenta Preservative Free Review and Sufenta Preservative Free Label ), NORMACOL (BACTRIM) (View Normacol (bactrim) Review and Normacol (bactrim) Label ), DEXAMETHASON MERCK (DEXAMETHASONE SODIUM PHOSPHATE) (View Dexamethason Merck (dexamethasone Sodium Phosphate) Review and Dexamethason Merck (dexamethasone Sodium Phosphate) Label ), ACUPAN (View Acupan Review and Acupan Label ), BETADINE (View Betadine Review and Betadine Label ), NAROPEINE (ROPIVACAINE HYDROCHLORIDE) (View Naropeine (ropivacaine Hydrochloride) Review and Naropeine (ropivacaine Hydrochloride) Label ), DROPERIDOL (View Droperidol Review and Droperidol Label ). Patient was hospitalized.

6861095-9 | Procedural Hypotension
on Jul 07, 2010 Female patient from JAPAN , 61 years of age, weighting 92.59 lb, was diagnosed with induction of anaesthesia, local anaesthesia and was treated with Propofol (View Usage). Patient experienced the following unwanted or unexpected effects: procedural hypotension. Propofol dosage: Target Blood Concentration 4.0 Ug/ml. During the same period patient was treated with FENTANYL (View Fentanyl Review and Fentanyl Label ), LIDOCAINE (6 Ml) (View Lidocaine Review and Lidocaine Label ), DOXAZOSIN (From 0.25 Mg Up To 0.5 Mg Per Day) (View Doxazosin Review and Doxazosin Label ).

6856868-2 | Haematuria, Renal Failure Acute
Patient was taking Propofol (View Usage). Patient had the following side effects: haematuria, renal failure acute on Jun 30, 2010 from FRANCE Additional patient health information: Female patient , 17 years of age, was diagnosed with induction of anaesthesia and. Propofol dosage: Intravenous. During the same period patient was treated with ATRACURIUM BESYLATE (View Atracurium Besylate Review and Atracurium Besylate Label ), SUFENTA (SUFENTANIL CITRATE) (SUFENTANIL CITRATE) (View Sufenta (sufentanil Citrate) (sufentanil Citrate) Review and Sufenta (sufentanil Citrate) (sufentanil Citrate) Label ), NEURONTIN (View Neurontin Review and Neurontin Label ), BETADINE (POVIDONE IODINE) (POVIDONE IODINE) (View Betadine (povidone-iodine) (povidone-iodine) Review and Betadine (povidone-iodine) (povidone-iodine) Label ), NAROPEINE (ROPIVACAINE HYDROCHLORIDE) (ROPIVACAINE HYDROCHLORIDE) (View Naropeine (ropivacaine Hydrochloride) (ropivacaine Hydrochloride) Review and Naropeine (ropivacaine Hydrochloride) (ropivacaine Hydrochloride) Label ), DROLEPTAN (DROPERIDOL) (DROPERIDOL) (View Droleptan (droperidol) (droperidol) Review and Droleptan (droperidol) (droperidol) Label ), LOVENOX (HEPARIN FRACTION, SODIUM SALT) (HEPARIN FRACTION, SODIUM SALT (View Lovenox (heparin-fraction, Sodium Salt) (heparin-fraction, Sodium Salt Review and Lovenox (heparin-fraction, Sodium Salt) (heparin-fraction, Sodium Salt Label ), KETAMINE (KETAMINE) (KETAMINE) (View Ketamine (ketamine) (ketamine) Review and Ketamine (ketamine) (ketamine) Label ). Patient was hospitalized.