Mucodyne Side Effects|
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Mucodyne Adverse Effect Reports (FDA)
Showing 1-25 of 64 Next Page >
Cardio-respiratory Arrest, Pneumonia, Condition Aggravated (8474895-9)
on Jun 12, 2012 Male patient from JAPAN , 89 years of age, was treated with Mucodyne (carbocisteine)(View Usage). Patient experienced the following unwanted or unexpected effects: cardio-respiratory arrest, pneumonia (What is pneumonia?), condition aggravated. Mucodyne (carbocisteine) dosage: N/A.
Patient was taking other medications:
Pancytopenia (8453562-1)
Patient was taking Mucodyne (View Usage). Patient had the following side effects: pancytopenia on Jun 13, 2012 from JAPAN Additional patient health information: Female patient , 37 years of age, weighting 100.3 lb, . Mucodyne dosage: Daily Dose 1500 Mg.
Patient was taking other medications:
Pulmonary Congestion, Nasopharyngitis, Cough (8445852-3)
Adverse event was reported on Jun 14, 2012 by a Female patient taking Mucodyne (View Usage) (Dosage: N/A) . Location: JAPAN , 25 years of age, After Mucodyne was administered, patient had the following side effects: pulmonary congestion, nasopharyngitis, cough.
Patient was taking other medications:
Pneumonia Bacterial, Lung Disorder, Interstitial Lung Disease (8443505-9)
on Jun 07, 2012 Female patient from JAPAN , weighting 63.93 lb, was diagnosed with
Patient was taking other medications:
Pyrexia, Malignant Pleural Effusion, Altered State Of Consciousness, Condition Aggravated, Electrocardiogram St-t Segment Abnormal, Bundle Branch Block Left, Respiratory Failure, Mouth Breathing, Lung Neoplasm Malignant (8406975-8)
on Jun 06, 2006 Male patient from JAPAN , 84 years of age, weighting 154.3 lb, was treated with Mucodyne (carbocisteine)(View Usage). Patient had the following side effects: pyrexia, malignant pleural effusion, altered state of consciousness, condition aggravated, electrocardiogram st-t segment abnormal, bundle branch block left, respiratory failure, mouth breathing, lung neoplasm malignant. Mucodyne (carbocisteine) dosage: N/A.
Patient was taking other medications:
Hypertension (8399077-0)
Patient was taking Mucodyne (carbocisteine) (View Usage). After Mucodyne was administered, patient had the following side effects: hypertension on May 23, 2012 from JAPAN Additional patient health information: Male patient , 73 years of age, . Mucodyne (carbocisteine) dosage: N/A.
Patient was taking other medications:
Hypogeusia (8398573-X)
Adverse event was reported on May 24, 2012 by a Male patient taking Mucodyne (View Usage) (Dosage: N/A) was diagnosed with
Patient was taking other medications:
Ocular Hyperaemia, Oral Pain, Erythema (8386190-7)
on May 16, 2012 Male patient from JAPAN , 65 years of age, weighting 157.0 lb, was treated with Mucodyne (View Usage). Patient had the following side effects: ocular hyperaemia, oral pain, erythema. Mucodyne dosage: N/A.
Patient was taking other medications:
Hypoaesthesia, Application Site Pain (8334174-7)
on Apr 30, 2012 Male patient from UNITED KINGDOM , 52 years of age, was treated with Mucodyne(View Usage). After Mucodyne was administered, patient had the following side effects: hypoaesthesia, application site pain. Mucodyne dosage: N/A.
Patient was taking other medications:
Liver Function Test Abnormal, Palmar-plantar Erythrodysaesthesia Syndrome, Amylase Increased, Hypertension, Mouth Haemorrhage, Hepatic Function Abnormal (8327898-9)
Patient was taking Mucodyne (View Usage). Patient experienced the following unwanted or unexpected effects: liver function test abnormal, palmar-plantar erythrodysaesthesia syndrome, amylase increased, hypertension, mouth haemorrhage, hepatic function abnormal on Apr 25, 2012 from JAPAN Additional patient health information: Male patient , 78 years of age, weighting 110.2 lb, . Mucodyne dosage: 2 Df (daily Dose), , Oral.
Patient was taking other medications:
Myositis (8250409-3)
Adverse event was reported on Mar 21, 2012 by a Female patient taking Mucodyne (View Usage) (Dosage: N/A) . Location: JAPAN , 90 years of age, Patient had the following side effects: myositis (What is myositis?).
Patient was taking other medications:
Palpitations, Overdose (8241116-1)
on Mar 23, 2012 Female patient from JAPAN , 25 years of age, was treated with Mucodyne (View Usage). After Mucodyne was administered, patient had the following side effects: palpitations, overdose. Mucodyne dosage: N/A.
Patient was taking other medications:
Bile Duct Cancer (8229718-X)
on Mar 14, 2012 Male patient from JAPAN , 76 years of age, weighting 187.4 lb, was treated with Mucodyne(View Usage). Patient experienced the following unwanted or unexpected effects: bile duct cancer. Mucodyne dosage: Dosage Is Uncertain During A Day..
Patient was taking other medications:
Agitation (8191125-6)
Patient was taking Mucodyne (View Usage). Patient had the following side effects: agitation on Feb 17, 2012 from JAPAN Additional patient health information: Male patient , weighting 68.34 lb, was diagnosed with
Patient was taking other medications:
Aggression (8187952-1)
Adverse event was reported on Feb 29, 2012 by a Male patient taking Mucodyne (View Usage) (Dosage: N/A) . Location: JAPAN , child 10 years of age, After Mucodyne was administered, patient had the following side effects: aggression.
Patient was taking other medications:
Liver Disorder, Hepatitis Fulminant (8163667-0)
on Feb 23, 2012 Female patient from JAPAN , weighting 79.37 lb, was diagnosed with
Patient was taking other medications:
Hearing Impaired (8163625-6)
on Feb 17, 2012 Female patient from JAPAN , 13 years of age, was treated with Mucodyne(View Usage). Patient had the following side effects: hearing impaired. Mucodyne dosage: 750 Mg, 1x/day.
Patient was taking other medications:
Small Intestinal Perforation, Diarrhoea, Diverticulum Intestinal, Malignant Tumour Excision (8141634-0)
Patient was taking Mucodyne (View Usage). After Mucodyne was administered, patient had the following side effects: small intestinal perforation, diarrhoea, diverticulum intestinal, malignant tumour excision on Feb 10, 2012 from JAPAN Additional patient health information: Male patient , 57 years of age, was diagnosed with
Patient was taking other medications:
Blood Pressure Decreased, Vomiting, Loss Of Consciousness, Facial Pain, Decreased Appetite, Dizziness, Nausea, Renal Impairment (8133532-3)
Adverse event was reported on Feb 08, 2012 by a Female patient taking Mucodyne (View Usage) (Dosage: 1000 Mg, 1x/day) was diagnosed with
Patient was taking other medications:
Petit Mal Epilepsy (8126377-1)
on Feb 03, 2012 Male patient from JAPAN , child 4 years of age, weighting 35.27 lb, was treated with Mucodyne (View Usage). Patient had the following side effects: petit mal epilepsy. Mucodyne dosage: N/A.
Patient was taking other medications:
Interstitial Lung Disease (8113991-2)
on Jan 27, 2012 Male patient from JAPAN , 70 years of age, was treated with Mucodyne(View Usage). After Mucodyne was administered, patient had the following side effects: interstitial lung disease. Mucodyne dosage: N/A.
Patient was taking other medications:
Lung Neoplasm Malignant, Bronchitis (8096347-0)
Patient was taking Mucodyne (View Usage). Patient experienced the following unwanted or unexpected effects: lung neoplasm malignant, bronchitis (What is bronchitis?) on Jan 18, 2012 from JAPAN Additional patient health information: Male patient , 65 years of age, . Mucodyne dosage: Total Daily Dose : 1500 Mg.
Patient was taking other medications:
Petit Mal Epilepsy (8063806-6)
Adverse event was reported on Jan 13, 2012 by a Male patient taking Mucodyne (View Usage) (Dosage: N/A) . Location: JAPAN , child 4 years of age, weighting 35.27 lb, Patient had the following side effects: petit mal epilepsy.
Patient was taking other medications:
Conjunctival Haemorrhage, Urticaria (8051269-6)
on Jan 12, 2012 Female patient from JAPAN , child 3 years of age, weighting 29.98 lb, was diagnosed with
Patient was taking other medications:
Dizziness, Vomiting, Irritability, Alopecia, Personality Change, Gait Disturbance, Salivary Hypersecretion, Impulsive Behaviour, Stress (8021004-6)
on Dec 15, 2011 Female patient from JAPAN , 17 years of age, weighting 89.95 lb, was treated with Mucodyne Dry Syrup 50% (l-carbocisteine)(View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), vomiting, irritability, alopecia, personality change, gait disturbance, salivary hypersecretion, impulsive behaviour, stress (What is stress?). Mucodyne Dry Syrup 50% (l-carbocisteine) dosage: N/A.
Patient was taking other medications:
on Jun 12, 2012 Male patient from JAPAN , 89 years of age, was treated with Mucodyne (carbocisteine)(View Usage). Patient experienced the following unwanted or unexpected effects: cardio-respiratory arrest, pneumonia (What is pneumonia?), condition aggravated. Mucodyne (carbocisteine) dosage: N/A.
Patient was taking other medications:
- MAGLAX (MAGNESSIUM OXIDE) (View Maglax (magnessium Oxide) Review and Maglax (magnessium Oxide) Label )
- CASODEX (View Casodex Review and Casodex Label )
- NU LOTAN (LOARTAN POTASSIUM) (View Nu-lotan (loartan Potassium) Review and Nu-lotan (loartan Potassium) Label )
- SOL MELCORT (METHYLPREDNISOLONE SODIUM SUCCINATE) (View Sol-melcort (methylprednisolone Sodium Succinate) Review and Sol-melcort (methylprednisolone Sodium Succinate) Label )
- ROZEREM (8 Mg (8 Mg, 1 In 1 D), Per Oral) (View Rozerem Review and Rozerem Label )
- FLIVAS OD (NAFTOPIDIL) (View Flivas Od (naftopidil) Review and Flivas Od (naftopidil) Label )
- LENDEM D (BROTIZOLAM) (View Lendem D (brotizolam) Review and Lendem D (brotizolam) Label )
- SULBACILLIN (AMPICILLIN SODIUM, SULBACTAM SODIUM) (View Sulbacillin (ampicillin Sodium, Sulbactam Sodium) Review and Sulbacillin (ampicillin Sodium, Sulbactam Sodium) Label )
Pancytopenia (8453562-1)
Patient was taking Mucodyne (View Usage). Patient had the following side effects: pancytopenia on Jun 13, 2012 from JAPAN Additional patient health information: Female patient , 37 years of age, weighting 100.3 lb, . Mucodyne dosage: Daily Dose 1500 Mg.
Patient was taking other medications:
- ADONA (Daily Dose 90 Mg) (View Adona Review and Adona Label )
- KEPPRA (View Keppra Review and Keppra Label )
- MEILAX (Daily Dose 1 Mg) (View Meilax Review and Meilax Label )
- PANVITAN (Daily Dose 1 Gm) (View Panvitan Review and Panvitan Label )
- TRANSAMINE CAP (Daily Dose 750 Mg) (View Transamine Cap Review and Transamine Cap Label )
- CLOBAZAM (Daily Dose 20 Mg) (View Clobazam Review and Clobazam Label )
- LANSOPRAZOLE (Daily Dose 15 Mg) (View Lansoprazole Review and Lansoprazole Label )
- MAGMITT (Daily Dose 990 Mg) (View Magmitt Review and Magmitt Label )
Pulmonary Congestion, Nasopharyngitis, Cough (8445852-3)
Adverse event was reported on Jun 14, 2012 by a Female patient taking Mucodyne (View Usage) (Dosage: N/A) . Location: JAPAN , 25 years of age, After Mucodyne was administered, patient had the following side effects: pulmonary congestion, nasopharyngitis, cough.
Patient was taking other medications:
- ALDACTONE (50 Mg, Daily) (View Aldactone Review and Aldactone Label )
- CODEINE PHOSPHATE (View Codeine Phosphate Review and Codeine Phosphate Label )
- GARENOXACIN MESILATE (View Garenoxacin Mesilate Review and Garenoxacin Mesilate Label )
- FLOMOX (View Flomox Review and Flomox Label )
Pneumonia Bacterial, Lung Disorder, Interstitial Lung Disease (8443505-9)
on Jun 07, 2012 Female patient from JAPAN , weighting 63.93 lb, was diagnosed with
- supportive care
- colitis ulcerative
- gastrooesophageal reflux disease
Patient was taking other medications:
- REMICADE (First Dose) (View Remicade Review and Remicade Label )
- RABEPRAZOLE SODIUM (View Rabeprazole Sodium Review and Rabeprazole Sodium Label )
Pyrexia, Malignant Pleural Effusion, Altered State Of Consciousness, Condition Aggravated, Electrocardiogram St-t Segment Abnormal, Bundle Branch Block Left, Respiratory Failure, Mouth Breathing, Lung Neoplasm Malignant (8406975-8)
on Jun 06, 2006 Male patient from JAPAN , 84 years of age, weighting 154.3 lb, was treated with Mucodyne (carbocisteine)(View Usage). Patient had the following side effects: pyrexia, malignant pleural effusion, altered state of consciousness, condition aggravated, electrocardiogram st-t segment abnormal, bundle branch block left, respiratory failure, mouth breathing, lung neoplasm malignant. Mucodyne (carbocisteine) dosage: N/A.
Patient was taking other medications:
- UNASYN (View Unasyn Review and Unasyn Label )
- BROACT (CEFPIROME SULFATE) (View Broact (cefpirome Sulfate) Review and Broact (cefpirome Sulfate) Label )
- BISOLVON (BROMHEXINE HYDROCHLORIDE) (View Bisolvon (bromhexine Hydrochloride) Review and Bisolvon (bromhexine Hydrochloride) Label )
- PLETAL (100 Mg, Bid, Other) (View Pletal Review and Pletal Label )
- VALPROATE SODIUM (View Valproate Sodium Review and Valproate Sodium Label )
Hypertension (8399077-0)
Patient was taking Mucodyne (carbocisteine) (View Usage). After Mucodyne was administered, patient had the following side effects: hypertension on May 23, 2012 from JAPAN Additional patient health information: Male patient , 73 years of age, . Mucodyne (carbocisteine) dosage: N/A.
Patient was taking other medications:
- MIRABEGRON (50 Mg) (View Mirabegron Review and Mirabegron Label )
- TAMSULOSIN HCL (0.2 Mg) (View Tamsulosin Hcl Review and Tamsulosin Hcl Label )
- ZOLPIDEM (10 Mg) (View Zolpidem Review and Zolpidem Label )
- EVIPROSTAT (CHIMAPHILA UMBELLATA, EQUISETUM ARVENSE, MANGANESE CHLORID (View Eviprostat (chimaphila Umbellata, Equisetum Arvense, Manganese Chlorid Review and Eviprostat (chimaphila Umbellata, Equisetum Arvense, Manganese Chlorid Label )
- RABEPRAZOLE SODIUM (View Rabeprazole Sodium Review and Rabeprazole Sodium Label )
- GASMOTIN (MOSAPRIDE CITRATE) (View Gasmotin (mosapride Citrate) Review and Gasmotin (mosapride Citrate) Label )
- DOGMATYL (50 Mg) (View Dogmatyl Review and Dogmatyl Label )
- CEROCRAL (IFENPRODIL TARTRATE) (View Cerocral (ifenprodil Tartrate) Review and Cerocral (ifenprodil Tartrate) Label )
Hypogeusia (8398573-X)
Adverse event was reported on May 24, 2012 by a Male patient taking Mucodyne (View Usage) (Dosage: N/A) was diagnosed with
- sinusitis (What is sinusitis?)
- oropharyngeal discomfort
Patient was taking other medications:
- HANGEKOBOKUTO (View Hangekobokuto Review and Hangekobokuto Label )
- CLARITHROMYCIN (View Clarithromycin Review and Clarithromycin Label )
- ONON (View Onon Review and Onon Label )
Ocular Hyperaemia, Oral Pain, Erythema (8386190-7)
on May 16, 2012 Male patient from JAPAN , 65 years of age, weighting 157.0 lb, was treated with Mucodyne (View Usage). Patient had the following side effects: ocular hyperaemia, oral pain, erythema. Mucodyne dosage: N/A.
Patient was taking other medications:
- AMOXICILLIN (View Amoxicillin Review and Amoxicillin Label )
- CLARITHROMYCIN (View Clarithromycin Review and Clarithromycin Label )
- AMLODIPINE BESYLATE (View Amlodipine Besylate Review and Amlodipine Besylate Label )
- ALLEGRA (View Allegra Review and Allegra Label )
- HMG COA REDUCTASE INHIBITORS (View Hmg Coa Reductase Inhibitors Review and Hmg Coa Reductase Inhibitors Label )
- OLMESARTAN MEDOXOMIL (View Olmesartan Medoxomil Review and Olmesartan Medoxomil Label )
- EMPYNASE (View Empynase Review and Empynase Label )
Hypoaesthesia, Application Site Pain (8334174-7)
on Apr 30, 2012 Male patient from UNITED KINGDOM , 52 years of age, was treated with Mucodyne(View Usage). After Mucodyne was administered, patient had the following side effects: hypoaesthesia, application site pain. Mucodyne dosage: N/A.
Patient was taking other medications:
- DIPYRIDAMOL (View Dipyridamol Review and Dipyridamol Label )
- FLUTICASONE PROPIONATE/SALMETEROL (View Fluticasone Propionate/salmeterol Review and Fluticasone Propionate/salmeterol Label )
- SPIRIVA (View Spiriva Review and Spiriva Label )
- ALBUTEROL (View Albuterol Review and Albuterol Label )
- NICOTINE (View Nicotine Review and Nicotine Label )
Liver Function Test Abnormal, Palmar-plantar Erythrodysaesthesia Syndrome, Amylase Increased, Hypertension, Mouth Haemorrhage, Hepatic Function Abnormal (8327898-9)
Patient was taking Mucodyne (View Usage). Patient experienced the following unwanted or unexpected effects: liver function test abnormal, palmar-plantar erythrodysaesthesia syndrome, amylase increased, hypertension, mouth haemorrhage, hepatic function abnormal on Apr 25, 2012 from JAPAN Additional patient health information: Male patient , 78 years of age, weighting 110.2 lb, . Mucodyne dosage: 2 Df (daily Dose), , Oral.
Patient was taking other medications:
- NEXAVAR (400 Mg (daily Dose)) (View Nexavar Review and Nexavar Label )
Myositis (8250409-3)
Adverse event was reported on Mar 21, 2012 by a Female patient taking Mucodyne (View Usage) (Dosage: N/A) . Location: JAPAN , 90 years of age, Patient had the following side effects: myositis (What is myositis?).
Patient was taking other medications:
- ZOLPIDEM (View Zolpidem Review and Zolpidem Label )
- ETIZOLAM (View Etizolam Review and Etizolam Label )
- INDERAL (View Inderal Review and Inderal Label )
- CELEBREX (100 Mg, 2x/day) (View Celebrex Review and Celebrex Label )
- ALFAROL (View Alfarol Review and Alfarol Label )
- TRITEREN (View Triteren Review and Triteren Label )
- PRAVASTATIN (View Pravastatin Review and Pravastatin Label )
Palpitations, Overdose (8241116-1)
on Mar 23, 2012 Female patient from JAPAN , 25 years of age, was treated with Mucodyne (View Usage). After Mucodyne was administered, patient had the following side effects: palpitations, overdose. Mucodyne dosage: N/A.
Patient was taking other medications:
- FLUTICASONE PROPIONATE/SALMETEROL (14iuax Per Day) (View Fluticasone Propionate/salmeterol Review and Fluticasone Propionate/salmeterol Label )
- ZITHROMAX (View Zithromax Review and Zithromax Label )
Bile Duct Cancer (8229718-X)
on Mar 14, 2012 Male patient from JAPAN , 76 years of age, weighting 187.4 lb, was treated with Mucodyne(View Usage). Patient experienced the following unwanted or unexpected effects: bile duct cancer. Mucodyne dosage: Dosage Is Uncertain During A Day..
Patient was taking other medications:
- MUCOSTA (Dosage Is Uncertain During A Day.) (View Mucosta Review and Mucosta Label )
- MUCOSOLVAN (Dosage Is Uncertain During A Day.) (View Mucosolvan Review and Mucosolvan Label )
- DASEN (Dosage Is Uncertain During A Day.) (View Dasen Review and Dasen Label )
- LOXONIN (Dosage Is Uncertain During A Day.) (View Loxonin Review and Loxonin Label )
- ZETIA (Dose Not Changed) (View Zetia Review and Zetia Label )
- DOGMATYL (Dosage Is Uncertain During A Day.) (View Dogmatyl Review and Dogmatyl Label )
- ALPRAZOLAM (Dosage Is Uncertain During A Day.) (View Alprazolam Review and Alprazolam Label )
- PROTECADIN (The Divided Dose Frequency Is Uncertain.) (View Protecadin Review and Protecadin Label )
Agitation (8191125-6)
Patient was taking Mucodyne (View Usage). Patient had the following side effects: agitation on Feb 17, 2012 from JAPAN Additional patient health information: Male patient , weighting 68.34 lb, was diagnosed with
- nasopharyngitis
Patient was taking other medications:
- CLARITHROMYCIN (View Clarithromycin Review and Clarithromycin Label )
- ZESULAN (View Zesulan Review and Zesulan Label )
- RELENZA (10mg Per Day) (View Relenza Review and Relenza Label )
Aggression (8187952-1)
Adverse event was reported on Feb 29, 2012 by a Male patient taking Mucodyne (View Usage) (Dosage: N/A) . Location: JAPAN , child 10 years of age, After Mucodyne was administered, patient had the following side effects: aggression.
Patient was taking other medications:
- TULOBUTEROL (View Tulobuterol Review and Tulobuterol Label )
- RELENZA (20mg Per Day) (View Relenza Review and Relenza Label )
Liver Disorder, Hepatitis Fulminant (8163667-0)
on Feb 23, 2012 Female patient from JAPAN , weighting 79.37 lb, was diagnosed with
- rhinitis
Patient was taking other medications:
- SOLON (View Solon Review and Solon Label )
- PROTECADIN (View Protecadin Review and Protecadin Label )
- ZESULAN (View Zesulan Review and Zesulan Label )
- CLARITHROMYCIN (View Clarithromycin Review and Clarithromycin Label )
- PRONASE (View Pronase Review and Pronase Label )
Hearing Impaired (8163625-6)
on Feb 17, 2012 Female patient from JAPAN , 13 years of age, was treated with Mucodyne(View Usage). Patient had the following side effects: hearing impaired. Mucodyne dosage: 750 Mg, 1x/day.
Patient was taking other medications:
- LEFTOSE (30 Mg, 1x/day) (View Leftose Review and Leftose Label )
- ACETAMINOPHEN (200 Mg, As Needed) (View Acetaminophen Review and Acetaminophen Label )
- FLAVERIC (1.2 Mg, 1x/day) (View Flaveric Review and Flaveric Label )
Small Intestinal Perforation, Diarrhoea, Diverticulum Intestinal, Malignant Tumour Excision (8141634-0)
Patient was taking Mucodyne (View Usage). After Mucodyne was administered, patient had the following side effects: small intestinal perforation, diarrhoea, diverticulum intestinal, malignant tumour excision on Feb 10, 2012 from JAPAN Additional patient health information: Male patient , 57 years of age, was diagnosed with
- productive cough
- constipation prophylaxis
- hyperchlorhydria
Patient was taking other medications:
- PURSENNID /00142207/ (View Pursennid /00142207/ Review and Pursennid /00142207/ Label )
- RABEPRAZOLE SODIUM (View Rabeprazole Sodium Review and Rabeprazole Sodium Label )
- FOSRENOL (View Fosrenol Review and Fosrenol Label )
- CALCIUM CARBONATE (View Calcium Carbonate Review and Calcium Carbonate Label )
- ALLEGRA (View Allegra Review and Allegra Label )
Blood Pressure Decreased, Vomiting, Loss Of Consciousness, Facial Pain, Decreased Appetite, Dizziness, Nausea, Renal Impairment (8133532-3)
Adverse event was reported on Feb 08, 2012 by a Female patient taking Mucodyne (View Usage) (Dosage: 1000 Mg, 1x/day) was diagnosed with
- sinusitis (What is sinusitis?)
- hypertension
- facial pain
Patient was taking other medications:
- NORVASC (5 Mg, 1x/day) (View Norvasc Review and Norvasc Label )
- LYRICA (50 Mg, 2x/day) (View Lyrica Review and Lyrica Label )
Petit Mal Epilepsy (8126377-1)
on Feb 03, 2012 Male patient from JAPAN , child 4 years of age, weighting 35.27 lb, was treated with Mucodyne (View Usage). Patient had the following side effects: petit mal epilepsy. Mucodyne dosage: N/A.
Patient was taking other medications:
- INTAL (View Intal Review and Intal Label )
- PULMICORT 100 (View Pulmicort-100 Review and Pulmicort-100 Label )
- MEPTIN (View Meptin Review and Meptin Label )
- ZADITEN (View Zaditen Review and Zaditen Label )
- MUCOSOLVAN (View Mucosolvan Review and Mucosolvan Label )
- SINGULAIR (View Singulair Review and Singulair Label )
- CLARITIN (View Claritin Review and Claritin Label )
Interstitial Lung Disease (8113991-2)
on Jan 27, 2012 Male patient from JAPAN , 70 years of age, was treated with Mucodyne(View Usage). After Mucodyne was administered, patient had the following side effects: interstitial lung disease. Mucodyne dosage: N/A.
Patient was taking other medications:
- JANUVIA (View Januvia Review and Januvia Label )
- SPIRIVA (View Spiriva Review and Spiriva Label )
- CISPLATIN (View Cisplatin Review and Cisplatin Label )
- GRAMICIDIN S HYDROCHLORIDE AND NEOMYCIN SULFATE (View Gramicidin S Hydrochloride And Neomycin Sulfate Review and Gramicidin S Hydrochloride And Neomycin Sulfate Label )
- ETOPOSIDE (View Etoposide Review and Etoposide Label )
- LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label )
- FLUVASTATIN (View Fluvastatin Review and Fluvastatin Label )
- MAGNESIUM OXIDE (View Magnesium Oxide Review and Magnesium Oxide Label )
Lung Neoplasm Malignant, Bronchitis (8096347-0)
Patient was taking Mucodyne (View Usage). Patient experienced the following unwanted or unexpected effects: lung neoplasm malignant, bronchitis (What is bronchitis?) on Jan 18, 2012 from JAPAN Additional patient health information: Male patient , 65 years of age, . Mucodyne dosage: Total Daily Dose : 1500 Mg.
Patient was taking other medications:
- ALLOPURINOL (Total Daily Dose : 100 Mg) (View Allopurinol Review and Allopurinol Label )
- WYSTAL (Total Daily Dose : 1 G) (View Wystal Review and Wystal Label )
- AMSULMYLAN (Total Daily Dose : 3 Gm) (View Amsulmylan Review and Amsulmylan Label )
- NORVASC (Total Daily Dose : 5 Mg) (View Norvasc Review and Norvasc Label )
- KEPPRA (View Keppra Review and Keppra Label )
Petit Mal Epilepsy (8063806-6)
Adverse event was reported on Jan 13, 2012 by a Male patient taking Mucodyne (View Usage) (Dosage: N/A) . Location: JAPAN , child 4 years of age, weighting 35.27 lb, Patient had the following side effects: petit mal epilepsy.
Patient was taking other medications:
- ZADITEN (View Zaditen Review and Zaditen Label )
- MEPTIN (View Meptin Review and Meptin Label )
- MUCOSOLVAN (View Mucosolvan Review and Mucosolvan Label )
- PULMICORT 100 (View Pulmicort-100 Review and Pulmicort-100 Label )
- CLARITIN (View Claritin Review and Claritin Label )
- SINGULAIR (View Singulair Review and Singulair Label )
- INTAL (View Intal Review and Intal Label )
Conjunctival Haemorrhage, Urticaria (8051269-6)
on Jan 12, 2012 Female patient from JAPAN , child 3 years of age, weighting 29.98 lb, was diagnosed with
- pneumonia (What is pneumonia?)
- pharyngitis
- asthma (What is asthma?)
- gastrointestinal disorder
Patient was taking other medications:
- TRANSAMIN POWDER (View Transamin Powder Review and Transamin Powder Label )
- ONON (D) (View Onon Review and Onon Label )
- CEFAZOLIN SODIUM (View Cefazolin Sodium Review and Cefazolin Sodium Label )
- ANTIBIOTICS RESISTANT LACTIC ACID BACTERIAE (View Antibiotics-resistant Lactic Acid Bacteriae Review and Antibiotics-resistant Lactic Acid Bacteriae Label )
- CLARITHROMYCIN (View Clarithromycin Review and Clarithromycin Label )
Dizziness, Vomiting, Irritability, Alopecia, Personality Change, Gait Disturbance, Salivary Hypersecretion, Impulsive Behaviour, Stress (8021004-6)
on Dec 15, 2011 Female patient from JAPAN , 17 years of age, weighting 89.95 lb, was treated with Mucodyne Dry Syrup 50% (l-carbocisteine)(View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), vomiting, irritability, alopecia, personality change, gait disturbance, salivary hypersecretion, impulsive behaviour, stress (What is stress?). Mucodyne Dry Syrup 50% (l-carbocisteine) dosage: N/A.
Patient was taking other medications:
- BUPHENYL (13500 Mg;qd;po 10000 Mg;qd;po) (View Buphenyl Review and Buphenyl Label )
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Side Effects reported to FDA: 64. View All Mucodyne safety alerts: No Reported deaths: 11 Reported hospitalizations: 23
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