UPPER RESPIRATORY TRACT INFLAMMATION side effect
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Drugs associated with UPPER RESPIRATORY TRACT INFLAMMATION
ASPIRIN CELLCEPT CHAMPIX COZAAR DIOVAN MICARDIS PROPECIA REMICADE TAKEPRON VESICARE ZONISAMIDERemicade Side Effects Report #5455611-1
Physician from JAPAN reported REMICADE problem on Sept 07, 2007. Female patient, weighting 136.7 lb, was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: upper respiratory tract inflammation, . REMICADE dosage: unknown. Patient was hospitalized. Patient recovered.
Remicade Side Effects Report #5355081-8
REMICADE problem was reported by a Physician from JAPAN on June 01, 2007. Female patient, weighting 123.5 lb, was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: upper respiratory tract inflammation, . REMICADE dosage: unknown. Patient was hospitalized. Patient recovered.
Remicade Side Effects Report #5292096-2
Physician from JAPAN reported REMICADE problem on Mar 26, 2007. Female patient, weighting 123.5 lb, was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: upper respiratory tract inflammation, . REMICADE dosage: unknown. Patient was hospitalized. Patient recovered.
Cozaar Side Effects Report #5272984-3
COZAAR problem was reported by a Consumer or non-health professional from GREECE on Mar 07, 2007. Male patient, 73 years of age, was diagnosed with cardiac failure and was treated with COZAAR. After drug was administered, patient experienced the following problems/side effects: upper respiratory tract inflammation, . COZAAR dosage: unknown. Patient was hospitalized. Patient recovered.
Propecia Side Effects Report #5632166-X
Physician from JAPAN reported PROPECIA problem on Feb 13, 2008. Male patient, 32 years of age, weighting 167.6 lb, was diagnosed with androgenetic alopecia, upper respiratory tract inflammation and was treated with PROPECIA. After drug was administered, patient experienced the following problems/side effects: hydronephrosis, upper respiratory tract inflammation, urinary retention, . PROPECIA dosage: unknown. During the same period patient was treated with MEIACT, ASVERIN, AMBROXOL HYDROCHLORIDE, MIYA BM, ALUMINUM HYDROXIDE AND DIPOTASSIUM GLYCYRRHIZATE AND GLYCINE AND LEVOG. Patient was hospitalized. Patient recovered.
Aspirin Side Effects Report #5414994-9
ASPIRIN problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 10, 2007. Female patient, weighting 11.00 lb, was diagnosed with cardiac disorder and was treated with ASPIRIN. After drug was administered, patient experienced the following problems/side effects: hypoventilation, upper respiratory tract inflammation, . ASPIRIN dosage: AS USED: 20.25 MG UNIT DOSE: 20.25 MG. During the same period patient was treated with LASIX, PRILOSEC, FUROSEMIDE. Patient recovered.
Vesicare Side Effects Report #5401452-0
Physician from JAPAN reported VESICARE problem on July 09, 2007. Female patient, 84 years of age, weighting 156.5 lb, was diagnosed with hypertonic bladder and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: pyrexia, upper respiratory tract inflammation, urinary retention, . VESICARE dosage: 10 MG, UID/QD, ORAL. During the same period patient was treated with GASTER D ORODISPERSABLE CRLET, LIPITOR, AMLODIPINE BESYLATE, ASPIRIN, BLOPRESS, LASIX, ALFAROL. Patient was hospitalized. Patient recovered.
Vesicare Side Effects Report #5401452-0
VESICARE problem was reported by a Physician from JAPAN on July 09, 2007. Female patient, 84 years of age, weighting 156.5 lb, was diagnosed with hypertonic bladder and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: pyrexia, upper respiratory tract inflammation, urinary retention, . VESICARE dosage: 10 MG, UID/QD, ORAL. During the same period patient was treated with GASTER D ORODISPERSABLE CRLET, LIPITOR, AMLODIPINE BESYLATE, ASPIRIN, BLOPRESS, LASIX, ALFAROL. Patient was hospitalized. Patient recovered.
Zonisamide Side Effects Report #5786667-4
Physician from JAPAN reported ZONISAMIDE problem on June 05, 2008. Male patient, child 6 years of age, weighting 45.42 lb, was diagnosed with epilepsy, upper respiratory tract inflammation and was treated with ZONISAMIDE. After drug was administered, patient experienced the following problems/side effects: stevens-johnson syndrome, upper respiratory tract inflammation, . ZONISAMIDE dosage: unknown. During the same period patient was treated with TEGRETOL, ASVERIN, MUCODYNE, CEFZON, CALONAL. Patient was hospitalized. Patient recovered.
Propecia Side Effects Report #5374004-9
PROPECIA problem was reported by a Physician from JAPAN on June 18, 2007. Male patient, 51 years of age, weighting 70.55 lb, was diagnosed with male pattern baldness and was treated with PROPECIA. After drug was administered, patient experienced the following problems/side effects: hepatic function abnormal, upper respiratory tract inflammation, . PROPECIA dosage: unknown. Patient was hospitalized. Patient recovered.
Remicade Side Effects Report #5313870-X
Physician from JAPAN reported REMICADE problem on Apr 20, 2007. Female patient, weighting 119.0 lb, was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: peptic ulcer, upper respiratory tract inflammation, . REMICADE dosage: unknown. Patient was hospitalized. Patient recovered.
Aspirin Side Effects Report #5323404-1
ASPIRIN problem was reported by a Consumer or non-health professional from UNITED STATES on May 08, 2007. Female patient, weighting 11.00 lb, was diagnosed with cardiac disorder and was treated with ASPIRIN. After drug was administered, patient experienced the following problems/side effects: hypoventilation, upper respiratory tract inflammation, . ASPIRIN dosage: AS USED: 20.25 MG UNIT DOSE: 20.25 MG. During the same period patient was treated with LASIX, PRILOSEC, FUROSEMIDE. Patient recovered.
Remicade Side Effects Report #5334460-9
Physician from JAPAN reported REMICADE problem on May 16, 2007. Male patient, weighting 136.7 lb, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: tuberculous pleurisy, upper respiratory tract inflammation, . REMICADE dosage: unknown. During the same period patient was treated with RHEUMATREX. Patient was hospitalized. Patient recovered.
Remicade Side Effects Report #5297251-3
REMICADE problem was reported by a Physician from JAPAN on Apr 04, 2007. Male patient, weighting 136.7 lb, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: tuberculous pleurisy, upper respiratory tract inflammation, . REMICADE dosage: unknown. During the same period patient was treated with RHEUMATREX. Patient was hospitalized. Patient recovered.
Remicade Side Effects Report #5305516-1
Physician from JAPAN reported REMICADE problem on Apr 17, 2007. Male patient, weighting 136.7 lb, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: tuberculous pleurisy, upper respiratory tract inflammation, . REMICADE dosage: unknown. During the same period patient was treated with RHEUMATREX. Patient was hospitalized. Patient recovered.
Diovan Side Effects Report #5254904-0
DIOVAN problem was reported by a Pharmacist from JAPAN on Feb 20, 2007. Female patient was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, upper respiratory tract inflammation, . DIOVAN dosage: 40 MG/DAY. During the same period patient was treated with FIBRATES. Patient was hospitalized. Patient recovered.
Diovan Side Effects Report #5265977-3
Pharmacist from JAPAN reported DIOVAN problem on Mar 02, 2007. Female patient was diagnosed with hypertension and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, upper respiratory tract inflammation, . DIOVAN dosage: 40 MG/DAY. During the same period patient was treated with BEZATOL, LASIX, FIBRATES. Patient was hospitalized. Patient recovered.
Micardis Side Effects Report #5670003-8
MICARDIS problem was reported by a Consumer or non-health professional from JAPAN on Mar 14, 2008. Male patient, weighting 141.1 lb, was diagnosed with hypertension, prophylaxis and was treated with MICARDIS. After drug was administered, patient experienced the following problems/side effects: interstitial lung disease, respiratory failure, upper respiratory tract inflammation, . MICARDIS dosage: unknown. During the same period patient was treated with BONALON, MUCODYNE, PREDONINE, CLARITHROMYCIN, MAGNESIUM OXIDE, CODEINE SUL, ASPIRIN, OMEPRAL. Patient was hospitalized. Patient died on 04/01/2007.
Cellcept Side Effects Report #5629986-4
Health Professional from JAPAN reported CELLCEPT problem on Feb 06, 2008. Female patient, 50 years of age, was treated with CELLCEPT. After drug was administered, patient experienced the following problems/side effects: meningitis bacterial, multi-organ failure, upper respiratory tract inflammation, . CELLCEPT dosage: unknown. During the same period patient was treated with CYCLOSPORINE, METHYLPREDNISOLONE. Patient was hospitalized. Patient recovered.
Takepron Side Effects Report #5535124-9
TAKEPRON QD problem was reported by a Consumer or non-health professional from JAPAN on Nov 19, 2007. Female patient, 81 years of age, was diagnosed with reflux oesophagitis, fracture, pain and was treated with TAKEPRON QD. After drug was administered, patient experienced the following problems/side effects: agranulocytosis, sepsis, upper respiratory tract inflammation, . TAKEPRON QD dosage: 15 MG (15 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with HISRACK, WARFARIN, SELEBEX, SENEVACUL, LENDORMIN. Patient died.
Champix Side Effects Report #5718517-6
Health Professional from UNITED KINGDOM reported CHAMPIX problem on Apr 14, 2008. Female patient, 53 years of age, weighting 162.7 lb, was treated with CHAMPIX. After drug was administered, patient experienced the following problems/side effects: dyspnoea, obstructive airways disorder, upper respiratory tract inflammation, . CHAMPIX dosage: unknown. Patient was hospitalized. Patient recovered.
Remicade Side Effects Report #5292097-4
REMICADE problem was reported by a Physician from JAPAN on Mar 26, 2007. Female patient, weighting 103.6 lb, was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: hepatic function abnormal, pneumonia, upper respiratory tract inflammation, . REMICADE dosage: unknown. Patient was hospitalized. Patient recovered.