CONCOMITANT DISEASE AGGRAVATED side effect
What is CONCOMITANT DISEASE AGGRAVATED ?Drugs associated with CONCOMITANT DISEASE AGGRAVATED
BISOPROLOL CITALOPRAM CLOZAPINE CLOZARIL CYMBALTA DIPRIVAN ESCITALOPRAM FABRAZYME FERROUS HEPARIN INFLIXIMAB LEVONORGESTREL METFORMIN METHYLPREDNISOLO NATALIZUMAB NEORAL NICOTINE NORDITROPIN PREDNISOLONE PROGRAF RECLAST REMICADE TIOTROPIUM TRANSDERM ZELNORM ZYVOXCONCOMITANT DISEASE AGGRAVATED : Norditropin Side Effects Report #5616715-3
Physician from JAPAN reported NORDITROPIN NORDIFLEX problem on Jan 30, 2008. Male patient, child 12 years of age, weighting 68.34 lb, was diagnosed with langerhans' cell granulomatosis, osteoporosis, diabetes insipidus, rhinitis allergic, chronic sinusitis and was treated with NORDITROPIN NORDIFLEX. After drug was administered, patient experienced the following problems/side effects: concomitant disease aggravated, langerhans' cell granulomatosis, . NORDITROPIN NORDIFLEX dosage: unknown. During the same period patient was treated with ALFAROL, DESMOPRESSIN, EBASTEL, MUCODYNE, ZADITEN. Patient was hospitalized. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Remicade Side Effects Report #5628050-8
REMICADE problem was reported by a Health Professional from UNITED STATES on Feb 07, 2008. Female patient, weighting 296.7 lb, was diagnosed with crohn's disease and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: concomitant disease aggravated, crohn's disease, rash, . REMICADE dosage: unknown. Patient was hospitalized. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Norditropin Side Effects Report #5629433-2
Physician from JAPAN reported NORDITROPIN NORDIFLEX problem on Feb 06, 2008. Male patient, child 12 years of age, weighting 68.34 lb, was diagnosed with growth hormone deficiency, langerhans' cell granulomatosis, osteoporosis, diabetes insipidus, rhinitis allergic, chronic sinusitis and was treated with NORDITROPIN NORDIFLEX. After drug was administered, patient experienced the following problems/side effects: concomitant disease aggravated, langerhans' cell granulomatosis, . NORDITROPIN NORDIFLEX dosage: .75 MG, QD. During the same period patient was treated with NORDITROPIN NORDIFLEX, ALFAROL, DESMOPRESSIN, EBASTEL, MUCODYNE, ZADITEN. Patient was hospitalized. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Ferrous Side Effects Report #5590273-4
FERROUS SULPHATE problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 02, 2008. Female patient, 75 years of age, was diagnosed with anaemia and was treated with FERROUS SULPHATE. After drug was administered, patient experienced the following problems/side effects: concomitant disease aggravated, faeces discoloured, . FERROUS SULPHATE dosage: 160 MG, QD, ORAL. During the same period patient was treated with PLAVIX, AVANDIA, OXYCONTIN, PREVACID. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Nicotine Side Effects Report #5594379-5
Consumer or non-health professional from GERMANY reported NICOTINE problem on Jan 06, 2008. Male patient was treated with NICOTINE. After drug was administered, patient experienced the following problems/side effects: concomitant disease aggravated, headache, hypertension, nausea, palpitations, . NICOTINE dosage: 21 MG, QD, TRANSDERMAL. During the same period patient was treated with PULMICORT. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Nicotine Side Effects Report #5565858-1
NICOTINE problem was reported by a Physician from JAPAN on Dec 05, 2007. Male patient, 63 years of age, weighting 130.1 lb, was treated with NICOTINE. After drug was administered, patient experienced the following problems/side effects: concomitant disease aggravated, iiird nerve disorder, myasthenia gravis, . NICOTINE dosage: unknown. During the same period patient was treated with ASPIRIN, NORVASC, ENALAPRIL MALEATE, DOXAZOSIN MESYLATE. Patient was hospitalized. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Cymbalta Side Effects Report #5576240-5
Physician from UNITED STATES reported CYMBALTA problem on Dec 18, 2007. Male patient, 45 years of age, was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: concomitant disease aggravated, depression, fistula, radiation injury, throat cancer, . CYMBALTA dosage: unknown. During the same period patient was treated with FENTANYL, OXYCODONE, OXYCONTIN, FLAGYL, ERYTHROMYCIN, PROTONIX, LISINOPRIL, LITHIUM CARBONATE. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Neoral Side Effects Report #5524490-6
NEORAL problem was reported by a Consumer or non-health professional from AUSTRALIA on Nov 19, 2007. Male patient, child 6 years of age, was diagnosed with eczema and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: concomitant disease aggravated, multiple allergies, . NEORAL dosage: 0.2ML MANE, 0.3ML NOCTE. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Nicotine Side Effects Report #5526154-1
Physician from JAPAN reported NICOTINE problem on Nov 09, 2007. Male patient, 63 years of age, was treated with NICOTINE. After drug was administered, patient experienced the following problems/side effects: concomitant disease aggravated, diplopia, eyelid ptosis, myasthenia gravis, . NICOTINE dosage: 7 MG, QD, TRANSDERMAL. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Zyvox Side Effects Report #5502351-6
ZYVOX problem was reported by a Physician from JAPAN on Oct 18, 2007. Male patient, 84 years of age, was diagnosed with pneumonia staphylococcal and was treated with ZYVOX. After drug was administered, patient experienced the following problems/side effects: concomitant disease aggravated, platelet count decreased, . ZYVOX dosage: unknown. Patient died on 06/01/2007.
CONCOMITANT DISEASE AGGRAVATED : Natalizumab Side Effects Report #5448399-1
Health Professional from UNITED STATES reported NATALIZUMAB problem on Aug 28, 2007. Female patient, 56 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: concomitant disease aggravated, multiple sclerosis, . NATALIZUMAB dosage: 300 MG;QM;IV. Patient was hospitalized. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Ferrous Side Effects Report #5444445-X
FERROUS SULPHATE problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 16, 2007. Female patient, 76 years of age, was diagnosed with blood iron decreased and was treated with FERROUS SULPHATE. After drug was administered, patient experienced the following problems/side effects: concomitant disease aggravated, parkinson's disease, . FERROUS SULPHATE dosage: 160 MG, QD, ORAL. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Infliximab Side Effects Report #5380640-6
Pharmacist from UNITED KINGDOM reported INFLIXIMAB problem on June 26, 2007. Male patient, 14 years of age, weighting 74.96 lb, was diagnosed with crohn's disease and was treated with INFLIXIMAB. After drug was administered, patient experienced the following problems/side effects: concomitant disease aggravated, crohn's disease, grand mal convulsion, reversible posterior leukoencephalopathy syndrome, . INFLIXIMAB dosage: unknown. During the same period patient was treated with IMURAN, HYDROCORTISONE, OMEPRAZOLE. Patient was hospitalized. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Levonorgestrel Side Effects Report #5398009-7
LEVONORGESTREL problem was reported by a Health Professional from GERMANY on July 26, 2007. Female patient was diagnosed with contraception and was treated with LEVONORGESTREL. After drug was administered, patient experienced the following problems/side effects: concomitant disease aggravated, multiple sclerosis relapse, . LEVONORGESTREL dosage: unknown. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Clozaril Side Effects Report #5401105-9
Health Professional from NEW ZEALAND reported CLOZARIL problem on July 23, 2007. Male patient was diagnosed with obsessive-compulsive disorder and was treated with CLOZARIL. After drug was administered, patient experienced the following problems/side effects: concomitant disease aggravated, obsessive-compulsive disorder, . CLOZARIL dosage: 400 MG/DAY. During the same period patient was treated with FLUOXETINE. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Infliximab Side Effects Report #5380640-6
INFLIXIMAB problem was reported by a Pharmacist from UNITED KINGDOM on June 26, 2007. Male patient, 14 years of age, weighting 74.96 lb, was diagnosed with crohn's disease and was treated with INFLIXIMAB. After drug was administered, patient experienced the following problems/side effects: concomitant disease aggravated, crohn's disease, grand mal convulsion, reversible posterior leukoencephalopathy syndrome, . INFLIXIMAB dosage: unknown. During the same period patient was treated with IMURAN, HYDROCORTISONE, OMEPRAZOLE. Patient was hospitalized. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Levonorgestrel Side Effects Report #5398009-7
Health Professional from GERMANY reported LEVONORGESTREL problem on July 26, 2007. Female patient was diagnosed with contraception and was treated with LEVONORGESTREL. After drug was administered, patient experienced the following problems/side effects: concomitant disease aggravated, multiple sclerosis relapse, . LEVONORGESTREL dosage: unknown. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Clozaril Side Effects Report #5401105-9
CLOZARIL problem was reported by a Health Professional from NEW ZEALAND on July 23, 2007. Male patient was diagnosed with obsessive-compulsive disorder and was treated with CLOZARIL. After drug was administered, patient experienced the following problems/side effects: concomitant disease aggravated, obsessive-compulsive disorder, . CLOZARIL dosage: 400 MG/DAY. During the same period patient was treated with FLUOXETINE. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Nicotine Side Effects Report #5661107-4
Consumer or non-health professional from UNITED STATES reported NICOTINE problem on Feb 26, 2008. Male patient was treated with NICOTINE. After drug was administered, patient experienced the following problems/side effects: cardiac failure congestive, concomitant disease aggravated, . NICOTINE dosage: 21 MG, QD, TRANSDERMAL; 14 MG, QD, TRANSDERMAL; 14 MG, QD, TRANSDERMAL. Patient was hospitalized. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Heparin Side Effects Report #5669182-8
HEPARIN problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 17, 2008. Female patient, 53 years of age, weighting 185.0 lb, was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: alopecia, concomitant disease aggravated, dizziness, fatigue, headache, nausea, . HEPARIN dosage: unknown. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Metformin Side Effects Report #5679749-9
Consumer or non-health professional from GERMANY reported METFORMIN HYDROCHLORIDE problem on Mar 10, 2008. Male patient, 74 years of age, was treated with METFORMIN HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: cardiogenic shock, concomitant disease aggravated, continuous haemodiafiltration, diabetic nephropathy, dyspnoea, lactic acidosis, multi-organ failure, renal failure acute, . METFORMIN HYDROCHLORIDE dosage: unknown. Patient was hospitalized. Patient died.
CONCOMITANT DISEASE AGGRAVATED : Escitalopram Side Effects Report #5616212-5
ESCITALOPRAM problem was reported by a Consumer or non-health professional from SWEDEN on Jan 17, 2008. Male patient, 36 years of age, was diagnosed with pulmonary embolism and was treated with ESCITALOPRAM. After drug was administered, patient experienced the following problems/side effects: cerebral haemorrhage, concomitant disease aggravated, deep vein thrombosis, grand mal convulsion, hypertension, pulmonary embolism, treatment noncompliance, . ESCITALOPRAM dosage: 10MG QD PO. During the same period patient was treated with FRAGMIN, WARFARIN, SERETIDE DISKUS, VENTOLIN. Patient was hospitalized. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Nicotine Side Effects Report #5622853-1
Consumer or non-health professional from GERMANY reported NICOTINE problem on Jan 28, 2008. Male patient, 51 years of age, weighting 154.3 lb, was treated with NICOTINE. After drug was administered, patient experienced the following problems/side effects: blood pressure systolic increased, concomitant disease aggravated, dyspnoea, headache, heart rate increased, hypertension, nausea, palpitations, . NICOTINE dosage: 21 MG, QD, TRANSDERMAL. During the same period patient was treated with PULMICORT. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Nicotine Side Effects Report #5630672-5
NICOTINE problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 03, 2008. Male patient, 68 years of age, was treated with NICOTINE. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, concomitant disease aggravated, loss of consciousness, . NICOTINE dosage: 21MG, TRANSDERMAL 14MG, TRANSDERMAL. During the same period patient was treated with LIPITOR, CALCIUM CHANNEL BLOCKERS, METFORMIN, GLIMEPIRIDE. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Reclast Side Effects Report #5598167-5
Physician from UNITED STATES reported RECLAST problem on Jan 18, 2008. Female patient, 69 years of age, weighting 144.0 lb, was diagnosed with osteoporosis and was treated with RECLAST. After drug was administered, patient experienced the following problems/side effects: chills, concomitant disease aggravated, dyspnoea, emphysema, myalgia, pyrexia, . RECLAST dosage: unknown. During the same period patient was treated with XOPENEX, LITHIUM CARBONATE, ADVAIR DISKUS, PRIMIDONE, LEXAPRO, NEXIUM, PREDNISONE, MIRAPEX. Patient was hospitalized and became disabled. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Tiotropium Side Effects Report #5599023-9
TIOTROPIUM problem was reported by a Consumer or non-health professional from on Jan 16, 2008. Female patient, 64 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with TIOTROPIUM. After drug was administered, patient experienced the following problems/side effects: chronic obstructive pulmonary disease, concomitant disease aggravated, haemoptysis, . TIOTROPIUM dosage: unknown. During the same period patient was treated with TOLTERODINE TARTRATE, DIDRONEL, CACIT. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Reclast Side Effects Report #5602105-6
Physician from UNITED STATES reported RECLAST problem on Jan 21, 2008. Female patient, 69 years of age, weighting 144.0 lb, was diagnosed with osteoporosis and was treated with RECLAST. After drug was administered, patient experienced the following problems/side effects: chills, concomitant disease aggravated, dyspnoea, emphysema, myalgia, pyrexia, . RECLAST dosage: unknown. During the same period patient was treated with XOPENEX, LITHIUM CARBONATE, ADVAIR DISKUS, PRIMIDONE, LEXAPRO, NEXIUM, PREDNISONE, MIRAPEX. Patient was hospitalized and became disabled. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Nicotine Side Effects Report #5506786-7
NICOTINE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 25, 2007. Female patient, 46 years of age, weighting 123.0 lb, was treated with NICOTINE. After drug was administered, patient experienced the following problems/side effects: asthenia, concomitant disease aggravated, fatigue, menorrhagia, . NICOTINE dosage: 21 MG, QD, TRANSDERMAL. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Citalopram Side Effects Report #5482079-1
Health Professional from DENMARK reported CITALOPRAM HYDROBROMIDE problem on Sept 20, 2007. Male patient, 87 years of age, was treated with CITALOPRAM HYDROBROMIDE. After drug was administered, patient experienced the following problems/side effects: cardio-respiratory arrest, concomitant disease aggravated, cyanosis, panic attack, . CITALOPRAM HYDROBROMIDE dosage: 20 MG QD PO. During the same period patient was treated with DIPIPERON, HALDOL, ACETYLCYSTEINE, DEANXIT, LORAZEPAM, ASPIRIN. Patient died on 06/20/2007.
CONCOMITANT DISEASE AGGRAVATED : Fabrazyme Side Effects Report #5448434-0
FABRAZYME problem was reported by a Physician from JAPAN on Aug 27, 2007. Female patient, 48 years of age, weighting 114.6 lb, was diagnosed with fabry's disease and was treated with FABRAZYME. After drug was administered, patient experienced the following problems/side effects: cardiac failure, concomitant disease aggravated, pain in extremity, . FABRAZYME dosage: unknown. During the same period patient was treated with ENALAPRIL MALEATE, CARVEDILOL. Patient was hospitalized. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Bisoprolol Side Effects Report #5450849-1
Consumer or non-health professional from GERMANY reported BISOPROLOL problem on Sept 06, 2007. Female patient was diagnosed with musculoskeletal pain and was treated with BISOPROLOL. After drug was administered, patient experienced the following problems/side effects: amblyopia, concomitant disease aggravated, gait disturbance, vision blurred, . BISOPROLOL dosage: 2.5 MG, QD. During the same period patient was treated with AMLODIPINE, IMMUNOSPORIN, DECORTIN, ACTONEL PLUS CALCIUM, OMEPRAZOLE. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Prograf Side Effects Report #5451875-9
PROGRAF problem was reported by a Physician from JAPAN on Aug 31, 2007. Female patient, 24 years of age, weighting 94.80 lb, was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: bone marrow oedema, concomitant disease aggravated, embolism, leukaemia, pain, pain in extremity, pulmonary artery thrombosis, pulmonary haemorrhage, . PROGRAF dosage: 1.5 MG,. UID/QD, IV DRIP, 0.7 MG, D, IV DRIP,. Patient died on 04/08/2007.
CONCOMITANT DISEASE AGGRAVATED : Nicotine Side Effects Report #5408500-2
Consumer or non-health professional from UNITED STATES reported NICOTINE problem on July 26, 2007. Male patient, 61 years of age, was treated with NICOTINE. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, concomitant disease aggravated, . NICOTINE dosage: 21 MG, QD; TRANSDERMAL. During the same period patient was treated with CRESTOR, PREDNISONE, AUGMENTIN, FUROSEMIDE, HYDROZIDE, LISNOPRIL, OLANZAPINE, OMEPRAZOLE. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Methylprednisolo Side Effects Report #5381640-2
METHYLPREDNISOLONE problem was reported by a Consumer or non-health professional from JAPAN on June 27, 2007. Male patient, child 9 years of age, was diagnosed with nephrotic syndrome and was treated with METHYLPREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: chronic sinusitis, concomitant disease aggravated, nephrotic syndrome, . METHYLPREDNISOLONE dosage: unknown. During the same period patient was treated with CYCLOSPORINE. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Methylprednisolo Side Effects Report #5381717-1
Consumer or non-health professional from JAPAN reported METHYLPREDNISOLONE problem on June 27, 2007. Male patient, child 7 years of age, was diagnosed with nephrotic syndrome and was treated with METHYLPREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: chronic sinusitis, concomitant disease aggravated, nephrotic syndrome, . METHYLPREDNISOLONE dosage: unknown. During the same period patient was treated with CYCLOSPORINE. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Methylprednisolo Side Effects Report #5388969-2
METHYLPREDNISOLONE problem was reported by a Consumer or non-health professional from JAPAN on July 06, 2007. Male patient, child 9 years of age, was diagnosed with nephrotic syndrome and was treated with METHYLPREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: chronic sinusitis, concomitant disease aggravated, nephrotic syndrome, . METHYLPREDNISOLONE dosage: unknown. During the same period patient was treated with CYCLOSPORINE. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Prednisolone Side Effects Report #5388970-9
Consumer or non-health professional from JAPAN reported PREDNISOLONE problem on July 06, 2007. Male patient, child 7 years of age, was diagnosed with nephrotic syndrome and was treated with PREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: chronic sinusitis, concomitant disease aggravated, nasal congestion, nephrotic syndrome, purulence, . PREDNISOLONE dosage: unknown. During the same period patient was treated with CYCLOSPORINE. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Methylprednisolo Side Effects Report #5381640-2
METHYLPREDNISOLONE problem was reported by a Consumer or non-health professional from JAPAN on June 27, 2007. Male patient, child 9 years of age, was diagnosed with nephrotic syndrome and was treated with METHYLPREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: chronic sinusitis, concomitant disease aggravated, nephrotic syndrome, . METHYLPREDNISOLONE dosage: unknown. During the same period patient was treated with CYCLOSPORINE. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Methylprednisolo Side Effects Report #5381717-1
Consumer or non-health professional from JAPAN reported METHYLPREDNISOLONE problem on June 27, 2007. Male patient, child 7 years of age, was diagnosed with nephrotic syndrome and was treated with METHYLPREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: chronic sinusitis, concomitant disease aggravated, nephrotic syndrome, . METHYLPREDNISOLONE dosage: unknown. During the same period patient was treated with CYCLOSPORINE. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Methylprednisolo Side Effects Report #5388969-2
METHYLPREDNISOLONE problem was reported by a Consumer or non-health professional from JAPAN on July 06, 2007. Male patient, child 9 years of age, was diagnosed with nephrotic syndrome and was treated with METHYLPREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: chronic sinusitis, concomitant disease aggravated, nephrotic syndrome, . METHYLPREDNISOLONE dosage: unknown. During the same period patient was treated with CYCLOSPORINE. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Prednisolone Side Effects Report #5388970-9
Consumer or non-health professional from JAPAN reported PREDNISOLONE problem on July 06, 2007. Male patient, child 7 years of age, was diagnosed with nephrotic syndrome and was treated with PREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: chronic sinusitis, concomitant disease aggravated, nasal congestion, nephrotic syndrome, purulence, . PREDNISOLONE dosage: unknown. During the same period patient was treated with CYCLOSPORINE. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Diprivan Side Effects Report #5450847-8
DIPRIVAN problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 31, 2007. Female patient, 72 years of age, was diagnosed with anaesthesia and was treated with DIPRIVAN. After drug was administered, patient experienced the following problems/side effects: asthma, bronchospasm, concomitant disease aggravated, fatigue, no therapeutic response, . DIPRIVAN dosage: unknown. During the same period patient was treated with FLOVENT, VITAMIN B12, NOVALOG INSULIN, PREMARIN, PRILOSEC, VERAPAMIL, XANAX, ZOLOFT. Patient was hospitalized. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Zelnorm Side Effects Report #5467794-8
Physician from UNITED STATES reported ZELNORM problem on Sept 20, 2007. Female patient, 51 years of age, weighting 150.0 lb, was diagnosed with irritable bowel syndrome and was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: abdominal pain, cholecystectomy, concomitant disease aggravated, diarrhoea, dyspnoea, gallbladder disorder, . ZELNORM dosage: 6 MG, BID. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Clozapine Side Effects Report #5376825-5
CLOZAPINE problem was reported by a Health Professional from JAPAN on June 20, 2007. Male patient, 75 years of age, weighting 141.1 lb, was diagnosed with accidental exposure and was treated with CLOZAPINE. After drug was administered, patient experienced the following problems/side effects: abnormal behaviour, blood pressure decreased, concomitant disease aggravated, glossoptosis, oxygen saturation decreased, somnolence, speech disorder, . CLOZAPINE dosage: 100 MG, ONCE/SINGLE. During the same period patient was treated with ZOLPIDEM, PURSENNID, DECADRON, THYRADIN S, ASPIRIN, D ALFA, SELBEX, PARLODEL. Patient was hospitalized. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Transderm Side Effects Report #5391819-1
Consumer or non-health professional from UNITED STATES reported TRANSDERM SCOP problem on July 10, 2007. Female patient, 72 years of age, weighting 179.9 lb, was diagnosed with motion sickness and was treated with TRANSDERM SCOP. After drug was administered, patient experienced the following problems/side effects: atrioventricular block first degree, bundle branch block right, concomitant disease aggravated, confusional state, disorientation, memory impairment, qrs axis abnormal, . TRANSDERM SCOP dosage: 1.5 MG, ONCE/SINGLE, TRANSDERMAL. During the same period patient was treated with ZOLOFT, ANTIHYPERTENSIVE, REGLAN, ZANTAC, VIVELLE, NOVOLOG, NITRO, LANTUS. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Clozapine Side Effects Report #5376825-5
CLOZAPINE problem was reported by a Health Professional from JAPAN on June 20, 2007. Male patient, 75 years of age, weighting 141.1 lb, was diagnosed with accidental exposure and was treated with CLOZAPINE. After drug was administered, patient experienced the following problems/side effects: abnormal behaviour, blood pressure decreased, concomitant disease aggravated, glossoptosis, oxygen saturation decreased, somnolence, speech disorder, . CLOZAPINE dosage: 100 MG, ONCE/SINGLE. During the same period patient was treated with ZOLPIDEM, PURSENNID, DECADRON, THYRADIN S, ASPIRIN, D ALFA, SELBEX, PARLODEL. Patient was hospitalized. Patient recovered.
CONCOMITANT DISEASE AGGRAVATED : Transderm Side Effects Report #5391819-1
Consumer or non-health professional from UNITED STATES reported TRANSDERM SCOP problem on July 10, 2007. Female patient, 72 years of age, weighting 179.9 lb, was diagnosed with motion sickness and was treated with TRANSDERM SCOP. After drug was administered, patient experienced the following problems/side effects: atrioventricular block first degree, bundle branch block right, concomitant disease aggravated, confusional state, disorientation, memory impairment, qrs axis abnormal, . TRANSDERM SCOP dosage: 1.5 MG, ONCE/SINGLE, TRANSDERMAL. During the same period patient was treated with ZOLOFT, ANTIHYPERTENSIVE, REGLAN, ZANTAC, VIVELLE, NOVOLOG, NITRO, LANTUS. Patient recovered.