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BLOOD IMMUNOGLOBULIN E INCREASED side effect

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Ibuprofen Side Effects Report #5664525-3
Consumer or non-health professional from PORTUGAL reported IBUPROFEN problem on Feb 25, 2008. Male patient, 78 years of age, was diagnosed with arthralgia and was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, confusional state, extensor plantar response, headache, hypersensitivity, meningitis aseptic, nuchal rigidity, pyrexia, somnolence, . IBUPROFEN dosage: unknown. During the same period patient was treated with BISOPROLOL. Patient was hospitalized. Patient recovered.

Leuprolide Side Effects Report #5679874-2
LEUPROLIDE ACETATE problem was reported by a Consumer or non-health professional from JAPAN on Mar 19, 2008. Male patient, 74 years of age, was diagnosed with prostate cancer and was treated with LEUPROLIDE ACETATE. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, cell marker increased, disseminated intravascular coagulation, dyspnoea, interstitial lung disease, metastases to lung, pneumothorax, . LEUPROLIDE ACETATE dosage: 11.25 MG (11.25 MG, 1 IN 12 WK) SUBCUTANEOUS. During the same period patient was treated with CHLORMADINONE ACETATE. Patient was hospitalized. Patient died.

Ibuprofen Side Effects Report #5602091-9
Health Professional from UNITED STATES reported IBUPROFEN problem on Jan 15, 2008. Male patient, 78 years of age, was diagnosed with arthralgia, cardiac failure and was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, meningitis aseptic, . IBUPROFEN dosage: unknown. During the same period patient was treated with BISOPROLOL FUMARATE. Patient was hospitalized. Patient recovered.

Ibuprofen Side Effects Report #5603781-4
IBUPROFEN problem was reported by a Health Professional from UNITED STATES on Jan 07, 2008. Male patient, 78 years of age, was diagnosed with arthralgia and was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, confusional state, leukocytosis, meningitis aseptic, musculoskeletal stiffness, somnolence, . IBUPROFEN dosage: unknown. During the same period patient was treated with BISOPROLOL. Patient recovered.


Ibuprofen Side Effects Report #5606610-8
Health Professional from UNITED STATES reported IBUPROFEN problem on Jan 15, 2008. Male patient, 78 years of age, was diagnosed with arthralgia, cardiac failure and was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, meningitis aseptic, . IBUPROFEN dosage: unknown. During the same period patient was treated with BISOPROLOL FUMARATE. Patient was hospitalized. Patient recovered.

Ibuprofen Side Effects Report #5606618-2
IBUPROFEN problem was reported by a Health Professional from UNITED STATES on Jan 15, 2008. Male patient, 78 years of age, was diagnosed with arthralgia, cardiac failure and was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, meningitis aseptic, . IBUPROFEN dosage: unknown. During the same period patient was treated with BISOPROLOL FUMARATE. Patient was hospitalized. Patient recovered.

Clarithromycin Side Effects Report #5526227-3
Physician from JAPAN reported CLARITHROMYCIN problem on Nov 20, 2007. Male patient, 78 years of age, was diagnosed with pharyngitis, nail tinea, neuropathy peripheral, gastritis, anal fistula, insomnia and was treated with CLARITHROMYCIN. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, blood immunoglobulin g increased, blood immunoglobulin m increased, blood lactate dehydrogenase increased, c-reactive protein increased, eosinophil count increased, hyperhidrosis, lymphocyte morphology abnormal, . CLARITHROMYCIN dosage: 400 MG/D. During the same period patient was treated with HOCHUUEKKITOU, CONFATANIN, LAMISIL, MECOBALAMIN, MARZULENE S, NERIPROCT, DEPAS. Patient was hospitalized. Patient recovered.

Elaprase Side Effects Report #5485661-0
ELAPRASE problem was reported by a Consumer or non-health professional from JAPAN on Oct 03, 2007. Male patient, 42 years of age, weighting 103.6 lb, was diagnosed with mucopolysaccharidosis ii and was treated with ELAPRASE. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, depressed level of consciousness, headache, hypotension, infusion related reaction, nausea, pulse pressure decreased, syncope vasovagal, vomiting, . ELAPRASE dosage: 0.5 MG/KG, 1X/WK, IV DRIP. During the same period patient was treated with VERAPAMIL, OMEPRAZOLE, ACETYLSALICYLIC ACID SRT, DIGOXIN, TORSEMIDE, PIMOBENDAN, LEVOTHYROXINE, HYDROCORTISONE. Patient was hospitalized. Patient recovered.

Advil Side Effects Report #5407507-9
Health Professional from FRANCE reported ADVIL problem on Aug 02, 2007. Male patient, weighting 28.66 lb, was treated with ADVIL. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, erythema multiforme, tachycardia, . ADVIL dosage: unknown. During the same period patient was treated with CEFACLOR. Patient was hospitalized. Patient recovered.


Singulair Side Effects Report #5418305-4
SINGULAIR problem was reported by a Physician from UNITED STATES on Aug 07, 2007. Male patient, child 9 years of age, weighting 63.93 lb, was diagnosed with asthma, hypersensitivity and was treated with SINGULAIR. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, dermatitis atopic, pruritus, reaction to food additive, superinfection, . SINGULAIR dosage: unknown. During the same period patient was treated with BACTRIM. Patient was hospitalized and became disabled. Patient recovered.

Singulair Side Effects Report #5381949-2
Health Professional from UNITED STATES reported SINGULAIR problem on July 03, 2007. Male patient, child 9 years of age, was diagnosed with asthma, hypersensitivity and was treated with SINGULAIR. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, pruritus, skin atrophy, skin fissures, skin haemorrhage, . SINGULAIR dosage: unknown. During the same period patient was treated with BACTRIM. Patient was hospitalized and became disabled. Patient recovered.

Idursulfase Side Effects Report #5388697-3
IDURSULFASE problem was reported by a Consumer or non-health professional from JAPAN on June 27, 2007. Male patient, 42 years of age, weighting 103.6 lb, was diagnosed with mucopolysaccharidosis ii and was treated with IDURSULFASE. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, depressed level of consciousness, headache, hypotension, infusion related reaction, nausea, pulse pressure decreased, shock, vomiting, . IDURSULFASE dosage: (0.5 MG/KG, 1 IN 1WK), INTRAVENOUS DRIP. During the same period patient was treated with VERAPAMIL, OMEPRAZOLE, ASPIRIN, DIGOXIN, TORSEMIDE, PIMOBENDAN, LEVOTHYROXINE, HYDROCORTISONE. Patient was hospitalized. Patient recovered.

Rhinadvil Side Effects Report #5395538-7
Health Professional from FRANCE reported RHINADVIL problem on July 18, 2007. Female patient was diagnosed with rhinitis, pharyngitis and was treated with RHINADVIL. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, leukocytoclastic vasculitis, malaise, oedema peripheral, urticaria, . RHINADVIL dosage: unknown. During the same period patient was treated with MAXILASE. Patient was hospitalized. Patient recovered.

Singulair Side Effects Report #5381949-2
SINGULAIR problem was reported by a Health Professional from UNITED STATES on July 03, 2007. Male patient, child 9 years of age, was diagnosed with asthma, hypersensitivity and was treated with SINGULAIR. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, pruritus, skin atrophy, skin fissures, skin haemorrhage, . SINGULAIR dosage: unknown. During the same period patient was treated with BACTRIM. Patient was hospitalized and became disabled. Patient recovered.


Idursulfase Side Effects Report #5388697-3
Consumer or non-health professional from JAPAN reported IDURSULFASE problem on June 27, 2007. Male patient, 42 years of age, weighting 103.6 lb, was diagnosed with mucopolysaccharidosis ii and was treated with IDURSULFASE. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, depressed level of consciousness, headache, hypotension, infusion related reaction, nausea, pulse pressure decreased, shock, vomiting, . IDURSULFASE dosage: (0.5 MG/KG, 1 IN 1WK), INTRAVENOUS DRIP. During the same period patient was treated with VERAPAMIL, OMEPRAZOLE, ASPIRIN, DIGOXIN, TORSEMIDE, PIMOBENDAN, LEVOTHYROXINE, HYDROCORTISONE. Patient was hospitalized. Patient recovered.

Rhinadvil Side Effects Report #5395538-7
RHINADVIL problem was reported by a Health Professional from FRANCE on July 18, 2007. Female patient was diagnosed with rhinitis, pharyngitis and was treated with RHINADVIL. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, leukocytoclastic vasculitis, malaise, oedema peripheral, urticaria, . RHINADVIL dosage: unknown. During the same period patient was treated with MAXILASE. Patient was hospitalized. Patient recovered.

Carvedilol Side Effects Report #5771891-7
Consumer or non-health professional from FRANCE reported CARVEDILOL problem on June 10, 2008. Female patient, 77 years of age, was treated with CARVEDILOL. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, dermatitis exfoliative, dry skin, eczema, eosinophilia, eyelid oedema, lip oedema, lymphadenopathy, lymphoma, . CARVEDILOL dosage: 3.125MG TWICE PER DAY. During the same period patient was treated with ALDACTONE, ACETAMINOPHEN, HEMIGOXINE NATIVELLE, LASILIX, PERINDOPRIL ERBUMINE. Patient was hospitalized. Patient recovered.

Norditropin Side Effects Report #5778302-6
NORDITROPIN problem was reported by a Physician from TURKEY on June 08, 2008. Male patient, 25 years of age, weighting 81.57 lb, was diagnosed with hypopituitarism and was treated with NORDITROPIN. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, rash, . NORDITROPIN dosage: 1.7 MG, QD. During the same period patient was treated with PREGNYL. Patient recovered.

Micardis Side Effects Report #5786531-0
Physician from JAPAN reported MICARDIS problem on June 18, 2008. Male patient, weighting 156.5 lb, was diagnosed with hypertension, hyperlipidaemia, gastric ulcer, lumbar spinal stenosis, diabetes mellitus and was treated with MICARDIS. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, eosinophil count increased, . MICARDIS dosage: unknown. During the same period patient was treated with LIPITOR, ZANTAC, OPALMON, FLUITRAN, LIPLE, CONIEL, EUGLUCON, RENIVACE. Patient was hospitalized. Patient recovered.


Fabrazyme Side Effects Report #5796849-3
FABRAZYME problem was reported by a Physician from JAPAN on June 24, 2008. Male patient, 13 years of age, weighting 88.18 lb, was diagnosed with fabry's disease and was treated with FABRAZYME. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, cyanosis, dyspnoea, oxygen saturation decreased, . FABRAZYME dosage: 35 MG, Q2W, INTRAVENOUS. During the same period patient was treated with HYDROXYZINE, ACETAMINOPHEN, HYDROCORTISONE SUCCINATE, CARBAMAZEPINE, PRANLUKAST HYDRATE. Patient recovered.

Fabrazyme Side Effects Report #5738426-6
Physician from UNITED STATES reported FABRAZYME problem on Apr 29, 2008. Male patient, 38 years of age, weighting 205.0 lb, was diagnosed with fabry's disease and was treated with FABRAZYME. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, chest discomfort, dyspnoea, erythema, eye pruritus, eyelid oedema, rash maculo-papular, urticaria, . FABRAZYME dosage: 90 MG, Q2W, INTRAVENOUS. During the same period patient was treated with LORAZEPAM, TOPAMAX, PROZAC, OXYCONTIN. Patient recovered.

Lamisil Side Effects Report #5697460-5
LAMISIL problem was reported by a Physician from JAPAN on Mar 28, 2008. Male patient, 60 years of age, weighting 231.5 lb, was diagnosed with onychomycosis, hyperuricaemia, diabetes mellitus, hypertension, obesity and was treated with LAMISIL. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, computerised tomogram abnormal, dyspnoea, endotracheal intubation, haemoptysis, lung disorder, oxygen saturation decreased, pyrexia, white blood cell count increased, . LAMISIL dosage: 125 MG/ DAY. During the same period patient was treated with SELBEX, ALOSITOL, MIGLITOL, AMLODIN, BLOPRESS, ARTIST, SANOREX, GLYCORAN. Patient was hospitalized. Patient recovered.

Leuprolide Side Effects Report #5711399-8
Consumer or non-health professional from JAPAN reported LEUPROLIDE ACETATE problem on Apr 10, 2008. Male patient, 74 years of age, was diagnosed with prostate cancer and was treated with LEUPROLIDE ACETATE. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, cell marker increased, collagen disorder, disseminated intravascular coagulation, interstitial lung disease, surfactant protein increased, . LEUPROLIDE ACETATE dosage: 11.25MG (11.25 MG, 1 IN 12 WK); SUBCUTANEOUS. During the same period patient was treated with CHLORMADINONE ACETATE. Patient was hospitalized. Patient died.

Malarone Side Effects Report #5363606-1
MALARONE problem was reported by a Physician from FRANCE on June 19, 2007. Female patient, 40 years of age, was diagnosed with malaria prophylaxis and was treated with MALARONE. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, c-reactive protein increased, chest x-ray abnormal, cough, dyspnoea, eosinophil percentage abnormal, fatigue, hypersensitivity, hyperthermia, . MALARONE dosage: unknown. During the same period patient was treated with AUGMENTIN, TELITHROMYCIN. Patient was hospitalized. Patient recovered.

Xolair Side Effects Report #5364271-X
Physician from SWITZERLAND reported XOLAIR problem on June 08, 2007. Male patient was diagnosed with asthma and was treated with XOLAIR. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, bronchospasm, hypersensitivity, rhinitis, . XOLAIR dosage: 150 MG, UNK. Patient recovered.

Tresleen Side Effects Report #5320720-4
TRESLEEN problem was reported by a Physician from AUSTRIA on May 03, 2007. Male patient, child 10 years of age, was treated with TRESLEEN. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, . TRESLEEN dosage: unknown. Patient recovered.

Urso Side Effects Report #5263017-3
Consumer or non-health professional from JAPAN reported URSO problem on Mar 06, 2007. Male patient, 56 years of age, was diagnosed with hepatic function abnormal and was treated with URSO. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, eosinophil count increased, pleural effusion, pyrexia, . URSO dosage: 600MG QD PO. During the same period patient was treated with MERACAZOLE, LASIX, LIVACT, CARVEDILOL. Patient was hospitalized. Patient recovered.

Urso Side Effects Report #5294771-2
URSO problem was reported by a Consumer or non-health professional from JAPAN on Mar 22, 2007. Male patient, 56 years of age, was diagnosed with hepatic function abnormal and was treated with URSO. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin e increased, eosinophil count increased, pleural effusion, pyrexia, . URSO dosage: 600MG QD PO. During the same period patient was treated with MERCAZOLE, LASIX, LIVACT, CARVEDILOL. Patient was hospitalized. Patient recovered.

Allopurinol Side Effects Report #5657402-5
Health Professional from ITALY reported ALLOPURINOL problem on Feb 27, 2008. Male patient, 85 years of age, was diagnosed with hyperuricaemia, benign prostatic hyperplasia, hypertension and was treated with ALLOPURINOL. After drug was administered, patient experienced the following problems/side effects: biopsy skin, blood immunoglobulin e increased, dermatitis, gamma-glutamyltransferase increased, lichenoid keratosis, . ALLOPURINOL dosage: 300 MG/DAY. During the same period patient was treated with XATRAL, DIURESIX, COMBISARTAN. Patient was hospitalized. Patient recovered.

Propylthiouracil Side Effects Report #5635698-3
PROPYLTHIOURACIL problem was reported by a Consumer or non-health professional from TURKEY on Feb 11, 2008. Female patient, 43 years of age, was diagnosed with basedow's disease and was treated with PROPYLTHIOURACIL. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood immunoglobulin e increased, blood ph increased, breath sounds abnormal, eosinophil percentage increased, haemoglobin decreased, neutrophil percentage decreased, no therapeutic response, percussion test abnormal, . PROPYLTHIOURACIL dosage: unknown. Patient was hospitalized. Patient recovered.

Allopurinol Side Effects Report #5635947-1
Health Professional from ITALY reported ALLOPURINOL problem on Feb 14, 2008. Male patient, 85 years of age, was diagnosed with hyperuricaemia, benign prostatic hyperplasia, hypertension and was treated with ALLOPURINOL. After drug was administered, patient experienced the following problems/side effects: biopsy skin, blood immunoglobulin e increased, dermatitis, gamma-glutamyltransferase increased, lichenoid keratosis, . ALLOPURINOL dosage: 300 MG/DAY. During the same period patient was treated with XATRAL, DIURESIX, COMBISARTAN. Patient was hospitalized. Patient recovered.

Myozyme Side Effects Report #5614459-5
MYOZYME problem was reported by a Physician from UNITED STATES on Jan 21, 2008. Female patient, 37 years of age, weighting 112.2 lb, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: abdominal pain, blood immunoglobulin e increased, blood immunoglobulin g increased, chest discomfort, chest pain, dyspnoea, infusion related reaction, oedema peripheral, rash, . MYOZYME dosage: 20 MG/KG, Q2W, INTRAVENOUS. During the same period patient was treated with ACETAMINOPHEN, BENADRYL, TOPROL, CELEBREX, PAXIL. Patient recovered.

Yasmin Side Effects Report #5534200-4
Physician from UNITED STATES reported YASMIN problem on Nov 26, 2007. Female patient, 29 years of age, weighting 183.0 lb, was diagnosed with oral contraception, urticaria, back pain and was treated with YASMIN. After drug was administered, patient experienced the following problems/side effects: anticholinergic syndrome, blood immunoglobulin e increased, dry mouth, facial pain, flushing, palpitations, panic attack, pruritus, . YASMIN dosage: unknown. During the same period patient was treated with BENADRYL, CLARINEX, ALLEGRA, HYDROXYZINE, ZANTAC, SINGULAIR, DAYPRO, NAPROXEN. Patient recovered.

Furadantin Side Effects Report #5552121-8
FURADANTIN problem was reported by a Physician from FRANCE on Nov 26, 2007. Female patient, 81 years of age, was treated with FURADANTIN. After drug was administered, patient experienced the following problems/side effects: blood immunoglobulin a increased, blood immunoglobulin e increased, blood immunoglobulin g increased, blood immunoglobulin m increased, leukocytoclastic vasculitis, . FURADANTIN dosage: unknown. During the same period patient was treated with INEXIUM, TOPAAL, BACTRIM, LERCANIDIPINE. Patient was hospitalized. Patient recovered.

Lipitor Side Effects Report #5524170-7
Consumer or non-health professional from AUSTRALIA reported LIPITOR problem on Nov 15, 2007. Male patient, 45 years of age, was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: alopecia, blood immunoglobulin e increased, dermatitis allergic, dry skin, fatigue, hair disorder, lupus-like syndrome, muscle atrophy, photosensitivity reaction, . LIPITOR dosage: unknown. During the same period patient was treated with FISH OIL. Patient recovered.

Rifampicin Side Effects Report #5473352-1
RIFAMPICIN problem was reported by a Consumer or non-health professional from JAPAN on Sept 25, 2007. Male patient, 90 years of age, was diagnosed with tuberculosis, pulmonary tuberculosis, tuberculous pleurisy, gastrooesophageal reflux prophylaxis, cough, constipation prophylaxis and was treated with RIFAMPICIN. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase increased, blood immunoglobulin e increased, gamma-glutamyltransferase increased, idiopathic thrombocytopenic purpura, platelet count decreased, red blood cell count decreased, . RIFAMPICIN dosage: unknown. During the same period patient was treated with ISCOTIN, EBUTOL, TAGAMET, MUCODYNE, MUCOSOLVAN, CODIENE, MAGMITT. Patient was hospitalized. Patient recovered.

Singulair Side Effects Report #5389772-X
Physician from UNITED STATES reported SINGULAIR problem on July 11, 2007. Male patient, child 9 years of age, weighting 61.73 lb, was diagnosed with asthma, hypersensitivity and was treated with SINGULAIR. After drug was administered, patient experienced the following problems/side effects: adverse event, blood immunoglobulin e increased, pruritus, reaction to food additive, skin atrophy, skin fissures, skin haemorrhage, . SINGULAIR dosage: unknown. During the same period patient was treated with BACTRIM. Patient was hospitalized and became disabled. Patient recovered.

Singulair Side Effects Report #5402658-7
SINGULAIR problem was reported by a Health Professional from UNITED STATES on July 30, 2007. Male patient, weighting 64.00 lb, was diagnosed with asthma, hypersensitivity and was treated with SINGULAIR. After drug was administered, patient experienced the following problems/side effects: allergy to chemicals, blood immunoglobulin e increased, body temperature increased, eosinophil count increased, erythema, exposure to toxic agent, lymphadenopathy, nail discolouration, . SINGULAIR dosage: 5 MG ONCE PER DAY PO. Patient was hospitalized. Patient recovered.

Singulair Side Effects Report #5389772-X
Physician from UNITED STATES reported SINGULAIR problem on July 11, 2007. Male patient, child 9 years of age, weighting 61.73 lb, was diagnosed with asthma, hypersensitivity and was treated with SINGULAIR. After drug was administered, patient experienced the following problems/side effects: adverse event, blood immunoglobulin e increased, pruritus, reaction to food additive, skin atrophy, skin fissures, skin haemorrhage, . SINGULAIR dosage: unknown. During the same period patient was treated with BACTRIM. Patient was hospitalized and became disabled. Patient recovered.

Singulair Side Effects Report #5402658-7
SINGULAIR problem was reported by a Health Professional from UNITED STATES on July 30, 2007. Male patient, weighting 64.00 lb, was diagnosed with asthma, hypersensitivity and was treated with SINGULAIR. After drug was administered, patient experienced the following problems/side effects: allergy to chemicals, blood immunoglobulin e increased, body temperature increased, eosinophil count increased, erythema, exposure to toxic agent, lymphadenopathy, nail discolouration, . SINGULAIR dosage: 5 MG ONCE PER DAY PO. Patient was hospitalized. Patient recovered.

Oxytocin Side Effects Report #5786001-X
Health Professional from ITALY reported OXYTOCIN problem on June 23, 2008. Female patient, 33 years of age, was diagnosed with caesarean section and was treated with OXYTOCIN. After drug was administered, patient experienced the following problems/side effects: acute pulmonary oedema, blood immunoglobulin e increased, brain oedema, bronchospasm, cardiac arrest, chemical poisoning, endotracheal intubation, haemoglobin decreased, hypotension, . OXYTOCIN dosage: unknown. During the same period patient was treated with BUPIVACAINE. Patient was hospitalized. Patient died.

Heparin Side Effects Report #5691508-X
HEPARIN ECTION problem was reported by a Health Professional from UNITED STATES on Mar 19, 2008. Male patient, 50 years of age, weighting 237.0 lb, was diagnosed with haemodialysis and was treated with HEPARIN ECTION. After drug was administered, patient experienced the following problems/side effects: blood bicarbonate decreased, blood immunoglobulin e increased, blood lactate dehydrogenase increased, chest discomfort, condition aggravated, dyspnoea, erythema, oxygen saturation decreased, petechiae, . HEPARIN ECTION dosage: unknown. During the same period patient was treated with HEPARIN ECTION. Patient was hospitalized. Patient recovered.

Lamisil Side Effects Report #5714497-8
Physician from JAPAN reported LAMISIL problem on Apr 15, 2008. Male patient, 60 years of age, weighting 231.5 lb, was diagnosed with onychomycosis, hyperuricaemia, diabetes mellitus, hypertension, obesity and was treated with LAMISIL. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, blood immunoglobulin e increased, computerised tomogram abnormal, dyspnoea, endotracheal intubation, haemoptysis, interstitial lung disease, lung disorder, lymphocyte stimulation test positive, . LAMISIL dosage: 125 MG/ DAY. During the same period patient was treated with SELBEX, ALOSITOL, MIGLITOL, AMLODIN, BLOPRESS, ARTIST, SANOREX, GLYCORAN. Patient was hospitalized. Patient recovered.

Cefamezin Side Effects Report #5320229-8
CEFAMEZIN problem was reported by a Physician from JAPAN on May 01, 2007. Female patient, 50 years of age, was diagnosed with induction of anaesthesia and was treated with CEFAMEZIN. After drug was administered, patient experienced the following problems/side effects: anaphylactic reaction, blood immunoglobulin e increased, blood pressure decreased, endotracheal intubation complication, hypoxia, oxygen saturation decreased, respiratory arrest, . CEFAMEZIN dosage: unknown. During the same period patient was treated with PENTAZOCINE LACTATE, VECURONIUM BROMIDE, PROPOFOL, ATROPINE SULPHATE. Patient recovered.

Lipitor Side Effects Report #5329060-0
Consumer or non-health professional from AUSTRALIA reported LIPITOR problem on May 08, 2007. Male patient, 45 years of age, was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: alopecia, blood immunoglobulin e increased, dermatitis allergic, dry skin, fatigue, hair disorder, muscle atrophy, photosensitivity reaction, rash papular, . LIPITOR dosage: unknown. During the same period patient was treated with FISH OIL. Patient recovered.

Zeldox Side Effects Report #5304983-7
ZELDOX problem was reported by a Physician from AUSTRALIA on Apr 16, 2007. Female patient, weighting 169.3 lb, was diagnosed with bipolar disorder and was treated with ZELDOX. After drug was administered, patient experienced the following problems/side effects: antibody test abnormal, blood immunoglobulin e increased, constipation, dyspepsia, oedema peripheral, . ZELDOX dosage: unknown. During the same period patient was treated with VALPROATE, FLUPENTIXOL, SEROQUEL, BENZOTROPINE, LORAZEPAM, ZUCLOPENTHIXOL DECANOATE, LEVOTHYROXINE. Patient recovered.

Isradipine Side Effects Report #5663428-8
Health Professional from CHILE reported ISRADIPINE problem on Mar 02, 2008. Male patient, 78 years of age, was diagnosed with hypertension and was treated with ISRADIPINE. After drug was administered, patient experienced the following problems/side effects: anaemia, blood folate decreased, blood immunoglobulin e increased, echography abnormal, hyperthyroidism, interstitial lung disease, pulmonary fibrosis, weight decreased, . ISRADIPINE dosage: 5 MG;PO. During the same period patient was treated with AMIODARONE, HYTACAND, FLECAINIDE ACETATE, NEO MERCAZOLE, CARBIMAZOLE, PROPYLTHIOURACIL, ERTHROCYTE CONCENTRATE. Patient recovered.

Ibuprofen Side Effects Report #5678681-4
IBUPROFEN problem was reported by a Consumer or non-health professional from SINGAPORE on Mar 10, 2008. Male patient, child 12 years of age, was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: anaphylactic reaction, angioedema, blood immunoglobulin e increased, bradycardia, respiratory rate increased, . IBUPROFEN dosage: 150 MG; X1; PO. Patient was hospitalized. Patient recovered.

Zometa Side Effects Report #5621599-3
Consumer or non-health professional from AUSTRIA reported ZOMETA problem on Feb 04, 2008. Female patient, 63 years of age, was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: anaemia, atrial fibrillation, blood immunoglobulin e increased, pericardial effusion, pleural effusion, . ZOMETA dosage: 4 MG, UNK. Patient recovered.

Zometa Side Effects Report #5621813-4
ZOMETA problem was reported by a Physician from AUSTRIA on Feb 04, 2008. Female patient, 63 years of age, was diagnosed with osteitis deformans and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: anaemia, atrial fibrillation, blood immunoglobulin e increased, metastatic gastric cancer, pericardial effusion, polyserositis, . ZOMETA dosage: 4 MG, UNK. Patient was hospitalized. Patient recovered.

Strattera Side Effects Report #5587326-3
Physician from NETHERLANDS reported STRATTERA problem on Jan 02, 2008. Male patient, weighting 110.2 lb, was diagnosed with sleep disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: abdominal distension, abdominal pain upper, blood immunoglobulin e increased, bronchial hyperreactivity, cystitis, dyspnoea, fatigue, flank pain, hyperventilation, . STRATTERA dosage: 25 MG, UNK. During the same period patient was treated with MELATONIN. Patient recovered.