HYPOAESTHESIA ORAL side effect
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Drugs associated with HYPOAESTHESIA ORAL
ABREVA ACETAMINOPHEN ACIPHEX ACTONEL ADVAIR ALEVE ALTACE APLISOL AREDIA ARTICAINE ATACAND AUGMENTIN AVELOX AVONEX BENADRYL BYETTA CAMPTOSAR CEFUROXIME CHANTIX CILOSTAZOL CLARITIN CLIMARA CLONAZEPAM COLCHICINE COLGATE COMBIVENT COMMIT CREST CRESTOR CYMBALTA DICLOFENAC DIFFERIN DILANTIN DIOVAN DURAGESIC EFFEXOR ELONTRIL ENBREL ENZASTAURIN ERBITUX ETONOGESTREL ETOPOSIDE EXJADE FENISTIL FLOMAX FOLINIC FOSAMAX HEPARIN HUMIRA HUMULIN HYDROCORTISONE HYDROCORTONE HYZAAR IMITREX INTERFERON INVEGA IRESSA IRINOTECAN ISOTRETINOIN ISOVUE JANUVIA LAMICTAL LAMISIL LEVAQUIN LEVOFLOXACIN LIGNOCAINE LISINOPRIL LISTERINE LUNESTA LYRICA MAALOX MAGNEVIST METROGEL MIRALAX MIRTAZAPINE NAVELBINE NEXIUM NICORETTE NICOTINE OPTIRAY ORENCIA PATADAY PAXIL PEPCID PLAVIX PREVIDENT PRIMACARE PRINIVIL PROCREST PROLASTIN PROPOFOL PULMICORT RANEXA RANITIDINE REBIF REDUCTIL RELPAX REMICADE REQUIP RESCULA REVLIMID ROZEREM SENSIPAR SEPTOCAINE SEROQUEL SINGULAIR SPIRIVA SYMBICORT SYMLIN TARGET TAXOL TEKTURNA THALOMID TRIAMINIC TUBERSOL ULTRAVIST VAGISTAT VALTREX VERAMYST VIOXX VYTORIN XOLAIR XYLOCAINE YASMIN ZETIA ZICAM ZITHROMAC ZOCOR ZOLEDRONIC ZOMETAMagnevist Side Effects Report #5648912-5
Health Professional from UNITED STATES reported MAGNEVIST problem on Feb 04, 2008. Male patient, 31 years of age, weighting 185.2 lb, was diagnosed with nuclear magnetic resonance imaging brain and was treated with MAGNEVIST. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, lip swelling, urticaria, . MAGNEVIST dosage: TOTAL DAILY DOSE: 17 ML UNIT DOSE: 17 ML. During the same period patient was treated with THYROID. Patient recovered.
Magnevist Side Effects Report #5649265-9
MAGNEVIST problem was reported by a Health Professional from UNITED STATES on Dec 11, 2007. Female patient was diagnosed with nuclear magnetic resonance imaging and was treated with MAGNEVIST. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, . MAGNEVIST dosage: UNIT DOSE: 19 ML. Patient recovered.
Cefuroxime Side Effects Report #5649289-1
Consumer or non-health professional from UNITED STATES reported CEFUROXIME problem on Mar 03, 2008. Female patient, 16 years of age, weighting 120.0 lb, was diagnosed with infectious mononucleosis and was treated with CEFUROXIME. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, lip swelling, oedema mouth, . CEFUROXIME dosage: unknown. Patient recovered.
Magnevist Side Effects Report #5649309-4
MAGNEVIST problem was reported by a Health Professional from UNITED STATES on Dec 11, 2007. Female patient was diagnosed with nuclear magnetic resonance imaging and was treated with MAGNEVIST. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, . MAGNEVIST dosage: UNIT DOSE: 12 ML. Patient recovered.
Aleve Side Effects Report #5658410-0
Consumer or non-health professional from UNITED STATES reported ALEVE problem on Oct 16, 2007. Female patient, 70 years of age, weighting 160.9 lb, was diagnosed with back pain and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, paraesthesia oral, . ALEVE dosage: TOTAL DAILY DOSE: 220 MG UNIT DOSE: 220 MG. Patient recovered.
Remicade Side Effects Report #5664400-4
REMICADE problem was reported by a Health Professional from CANADA on Mar 05, 2008. Female patient, 47 years of age, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, paraesthesia, urine output increased, . REMICADE dosage: unknown. During the same period patient was treated with ARAVA, PREDNISONE, PREMARIN, TYLENOL, ADVIL. Patient recovered.
Optiray Side Effects Report #5671759-0
Health Professional from IRELAND reported OPTIRAY problem on Mar 10, 2008. Female patient was diagnosed with computerised tomogram and was treated with OPTIRAY. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, oedema mouth, . OPTIRAY dosage: 90 ML, SINGLE. Patient was hospitalized. Patient recovered.
Atacand Side Effects Report #5680523-8
ATACAND problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 24, 2008. Female patient, 66 years of age, was treated with ATACAND. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, paraesthesia, rash, . ATACAND dosage: unknown. During the same period patient was treated with CRESTOR. Patient recovered.
Heparin Side Effects Report #5613020-6
Consumer or non-health professional from UNITED STATES reported HEPARIN problem on Jan 25, 2008. Female patient, 54 years of age, weighting 127.9 lb, was diagnosed with haemodialysis, hypertension, blood cholesterol, laxative supportive care, asthma, diabetes mellitus and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, paraesthesia, pharyngeal hypoaesthesia, vomiting, . HEPARIN dosage: unknown. During the same period patient was treated with LOTREL, GEMFIBROZIL, LOPRESSOR, COLACE, FORMOTERAL, GLIMEPIRIDE. Patient recovered.
Climara Side Effects Report #5616410-0
CLIMARA PRO problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 26, 2007. Female patient, 52 years of age, weighting 158.7 lb, was diagnosed with osteoporosis and was treated with CLIMARA PRO. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, paraesthesia oral, pruritus, . CLIMARA PRO dosage: unknown. During the same period patient was treated with LEVOTHYROXINE, CALCIUM GLUCONATE. Patient recovered.
Climara Side Effects Report #5616454-9
Consumer or non-health professional from UNITED STATES reported CLIMARA PRO problem on Nov 26, 2007. Female patient, 52 years of age, weighting 158.7 lb, was diagnosed with osteoporosis and was treated with CLIMARA PRO. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, paraesthesia oral, pruritus, . CLIMARA PRO dosage: unknown. During the same period patient was treated with LEVOTHYROXINE, CALCIUM GLUCONATE. Patient recovered.
Hyzaar Side Effects Report #5626258-9
HYZAAR problem was reported by a Consumer or non-health professional from JAPAN on Jan 30, 2008. Female patient, 60 years of age, was diagnosed with hypertension and was treated with HYZAAR. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, . HYZAAR dosage: unknown. During the same period patient was treated with NORVASC. Patient recovered.
Heparin Side Effects Report #5629151-0
Consumer or non-health professional from UNITED STATES reported HEPARIN problem on Jan 04, 2008. Female patient, 23 years of age, weighting 101.4 lb, was diagnosed with prophylaxis and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, paraesthesia oral, . HEPARIN dosage: unknown. During the same period patient was treated with CHLORIDE. Patient recovered.
Heparin Side Effects Report #5629153-4
HEPARIN problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 08, 2008. Female patient, 38 years of age, weighting 134.5 lb, was diagnosed with thrombosis prophylaxis, haemodialysis and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, paraesthesia oral, . HEPARIN dosage: unknown. During the same period patient was treated with CHLORIDE. Patient recovered.
Heparin Side Effects Report #5640325-5
Pharmacist from UNITED STATES reported HEPARIN problem on Jan 04, 2008. Female patient, 23 years of age, weighting 101.4 lb, was diagnosed with prophylaxis and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, paraesthesia oral, . HEPARIN dosage: unknown. During the same period patient was treated with CHLORIDE. Patient recovered.
Heparin Side Effects Report #5640403-0
HEPARIN problem was reported by a Pharmacist from UNITED STATES on Jan 25, 2008. Female patient, 54 years of age, weighting 127.9 lb, was diagnosed with haemodialysis, hypertension, blood cholesterol, laxative supportive care, asthma, diabetes mellitus and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, paraesthesia, pharyngeal hypoaesthesia, vomiting, . HEPARIN dosage: unknown. During the same period patient was treated with LOTREL, GEMFIBROZIL, LOPRESSOR, COLACE, FORMOTERAL, GLIMEPIRIDE. Patient recovered.
Heparin Side Effects Report #5640498-4
Pharmacist from UNITED STATES reported HEPARIN problem on Jan 08, 2008. Female patient, 38 years of age, weighting 134.5 lb, was diagnosed with thrombosis prophylaxis, haemodialysis and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, paraesthesia oral, . HEPARIN dosage: unknown. During the same period patient was treated with CHLORIDE. Patient recovered.
Nicorette Side Effects Report #5641206-3
NICORETTE problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 15, 2007. Male patient, 47 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, paraesthesia oral, . NICORETTE dosage: unknown. Patient recovered.
Valtrex Side Effects Report #5644677-1
Consumer or non-health professional from UNITED STATES reported VALTREX problem on May 18, 2007. Female patient, 39 years of age, was diagnosed with genital herpes and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, infectious mononucleosis, nasopharyngitis, pharyngolaryngeal pain, . VALTREX dosage: unknown. Patient recovered.
Aleve Side Effects Report #5585685-9
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 12, 2007. Female patient, 77 years of age, weighting 134.5 lb, was diagnosed with muscle strain and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, . ALEVE dosage: TOTAL DAILY DOSE: 220 MG UNIT DOSE: 220 MG. Patient recovered.
Revlimid Side Effects Report #5638237-6
Health Professional from UNITED STATES reported REVLIMID problem on Oct 31, 2007. Female patient, 59 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, paraesthesia oral, . REVLIMID dosage: 25 MG, 1 IN 1 D, ORAL. During the same period patient was treated with LOVENOX. Patient recovered.
Revlimid Side Effects Report #5645957-6
REVLIMID problem was reported by a Health Professional from UNITED STATES on Dec 10, 2007. Male patient, 56 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, neuropathy peripheral, . REVLIMID dosage: 20 MG, ON FOR 20 DAYS / OFF FOR 8 DAYS, ORAL. During the same period patient was treated with LYRICA, COUMADIN, DEXAMETHASONE. Patient recovered.
Byetta Side Effects Report #5649578-0
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Nov 13, 2007. Female patient, 65 years of age, weighting 155.9 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE, METFORMIN. Patient recovered.
Crestor Side Effects Report #5563445-2
CRESTOR problem was reported by a Consumer or non-health professional from UNITED STATES on May 14, 2007. Female patient, 54 years of age, weighting 142.0 lb, was diagnosed with blood cholesterol increased and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, muscular weakness, myalgia, nausea, . CRESTOR dosage: unknown. Patient recovered.
Remicade Side Effects Report #5573473-9
Physician from IRAN (ISLAMIC REPUBLIC OF) reported REMICADE problem on Dec 15, 2007. Male patient, 55 years of age, weighting 165.3 lb, was diagnosed with psoriasis, hypertension and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, infusion related reaction, skin hyperpigmentation, . REMICADE dosage: unknown. During the same period patient was treated with LOSARTAN POTASSIUM, AMLODIPINE, TICLOPIDINE, NITROGLYCERIN. Patient recovered.
Remicade Side Effects Report #5575938-2
REMICADE problem was reported by a Health Professional from CANADA on Dec 20, 2007. Female patient, weighting 187.4 lb, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, paraesthesia, urinary incontinence, urine output increased, . REMICADE dosage: unknown. During the same period patient was treated with ARAVA, PREMARIN, PREDNISONE. Patient recovered.
Veramyst Side Effects Report #5512261-6
Consumer or non-health professional from UNITED STATES reported VERAMYST problem on Aug 22, 2007. Male patient, 47 years of age, was treated with VERAMYST. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, oedema mouth, paraesthesia oral, tongue discolouration, . VERAMYST dosage: unknown. During the same period patient was treated with SYNTHROID, CADUET, HYZAAR. Patient recovered.
Zometa Side Effects Report #5524486-4
ZOMETA problem was reported by a Consumer or non-health professional from FRANCE on Nov 19, 2007. Male patient, 63 years of age, was diagnosed with breast cancer male and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, impaired healing, osteonecrosis, pain in jaw, wisdom teeth removal, . ZOMETA dosage: 4 MG, QMO. Patient recovered.
Primacare Side Effects Report #5528132-5
Health Professional from UNITED STATES reported PRIMACARE ONE CAPS THER problem on Nov 26, 2007. Female patient, 24 years of age, was treated with PRIMACARE ONE CAPS THER. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, . PRIMACARE ONE CAPS THER dosage: unknown. Patient recovered.
Augmentin Side Effects Report #5530267-8
AUGMENTIN problem was reported by a Consumer or non-health professional from UNITED STATES on May 29, 2007. Female patient, 48 years of age, was diagnosed with sinusitis and was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, rash, swelling, . AUGMENTIN dosage: unknown. During the same period patient was treated with ADVAIR DISKUS, VENTOLIN HFA, ORTHO, LEVOXYL, PREDNISONE. Patient recovered.
Actonel Side Effects Report #5556753-2
Physician from UNITED STATES reported ACTONEL problem on Sept 13, 2007. Female patient, 63 years of age, weighting 134.9 lb, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, oral infection, oral pain, osteomyelitis, osteonecrosis, purulent discharge, tooth extraction, . ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with FOSAMAX, LIPITOR, FLUOXETINE, COZAAR, GLYBURIDE, SINEMET. Patient recovered.
Fosamax Side Effects Report #5568616-7
FOSAMAX problem was reported by a Physician from UNITED STATES on Oct 11, 2006. Female patient, 77 years of age, was diagnosed with osteoporosis, scoliosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, oral pain, osteonecrosis, tooth fracture, . FOSAMAX dosage: 70 MG WKY PO. During the same period patient was treated with ASPIRIN. Patient recovered.
Byetta Side Effects Report #5580601-8
Health Professional from UNITED STATES reported BYETTA problem on July 24, 2007. Female patient, 55 years of age, was diagnosed with glucose tolerance impaired and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, paraesthesia oral, . BYETTA dosage: unknown. During the same period patient was treated with ACIPHEX. Patient recovered.
Nicotine Side Effects Report #5483630-8
NICOTINE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 02, 2007. Female patient, 42 years of age, weighting 200.0 lb, was treated with NICOTINE. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, visual acuity reduced, . NICOTINE dosage: 21 MG, QD, TRANSDERMAL. Patient recovered.
Advair Side Effects Report #5495980-X
Consumer or non-health professional from UNITED STATES reported ADVAIR DISKUS problem on Jan 05, 2007. Female patient was diagnosed with asthma and was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, . ADVAIR DISKUS dosage: unknown. Patient recovered.
Maalox Side Effects Report #5455961-9
MAALOX ANTIACID problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 08, 2007. Female patient, 35 years of age, weighting 200.0 lb, was diagnosed with stomach discomfort and was treated with MAALOX ANTIACID. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, . MAALOX ANTIACID dosage: unknown. During the same period patient was treated with ALBUTEROL. Patient recovered.
Abreva Side Effects Report #5461869-5
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Jan 04, 2007. Male patient, 22 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, lip pain, oral herpes, paraesthesia oral, . ABREVA dosage: unknown. Patient recovered.
Lamictal Side Effects Report #5468340-5
LAMICTAL problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 24, 2007. Female patient, 49 years of age, was diagnosed with bipolar disorder and was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, lip swelling, lymphadenopathy, paraesthesia oral, swollen tongue, vaginal haemorrhage, weight increased, . LAMICTAL dosage: 25MG PER DAY. During the same period patient was treated with THYROID. Patient recovered.
Elontril Side Effects Report #5406075-5
Pharmacist from GERMANY reported ELONTRIL problem on Aug 01, 2007. Female patient, 28 years of age, weighting 143.3 lb, was diagnosed with depression and was treated with ELONTRIL. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, paraesthesia oral, . ELONTRIL dosage: unknown. Patient recovered.
Target Side Effects Report #5388203-3
TARGET NICOTINE GUM problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 16, 2007. Female patient, 27 years of age, was treated with TARGET NICOTINE GUM. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, toothache, . TARGET NICOTINE GUM dosage: unknown. Patient recovered.
Remicade Side Effects Report #5391281-9
Health Professional from CANADA reported REMICADE problem on July 10, 2007. Female patient, 47 years of age, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, paraesthesia, urinary incontinence, urine output increased, . REMICADE dosage: unknown. During the same period patient was treated with ARAVA, PREMARIN, PREDNISONE, TYLENOL, ADVIL LIQUI. Patient recovered.
Target Side Effects Report #5388203-3
TARGET NICOTINE GUM problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 16, 2007. Female patient, 27 years of age, was treated with TARGET NICOTINE GUM. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, toothache, . TARGET NICOTINE GUM dosage: unknown. Patient recovered.
Remicade Side Effects Report #5391281-9
Health Professional from CANADA reported REMICADE problem on July 10, 2007. Female patient, 47 years of age, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, paraesthesia, urinary incontinence, urine output increased, . REMICADE dosage: unknown. During the same period patient was treated with ARAVA, PREMARIN, PREDNISONE, TYLENOL, ADVIL LIQUI. Patient recovered.
Relpax Side Effects Report #5774306-8
RELPAX problem was reported by a Pharmacist from SLOVENIA on June 04, 2008. Female patient, 22 years of age, was diagnosed with migraine and was treated with RELPAX. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, paraesthesia oral, . RELPAX dosage: unknown. During the same period patient was treated with ORAL CONTRACEPTIVE NOS. Patient recovered.
Symbicort Side Effects Report #5776781-1
Consumer or non-health professional from UNITED STATES reported SYMBICORT problem on Mar 26, 2008. Female patient, 55 years of age, weighting 130.1 lb, was diagnosed with asthma and was treated with SYMBICORT. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, pharyngeal hypoaesthesia, . SYMBICORT dosage: unknown. During the same period patient was treated with ALBUTEROL, FLEXERIL, DESONIDE. Patient recovered.
Spiriva Side Effects Report #5782317-1
SPIRIVA problem was reported by a Physician from JAPAN on June 20, 2008. Male patient, weighting 126.8 lb, was diagnosed with dyspnoea, prophylaxis against gastrointestinal ulcer, hypertension and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, hypogeusia, . SPIRIVA dosage: unknown. During the same period patient was treated with ASPIRIN, MUCOSTA, MICARDIS, XYLOCAINE. Patient recovered.
Ultravist Side Effects Report #5789630-2
Health Professional from UNITED STATES reported ULTRAVIST problem on May 30, 2008. Female patient, 65 years of age, was diagnosed with angiogram and was treated with ULTRAVIST. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, sensation of foreign body, urticaria, . ULTRAVIST dosage: TOTAL DAILY DOSE: 180 ML UNIT DOSE: 100 ML. Patient recovered.
Byetta Side Effects Report #5793807-X
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 12, 2008. Female patient, 74 years of age, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, . BYETTA dosage: unknown. Patient recovered.
Crest Side Effects Report #5735796-X
Consumer or non-health professional from UNITED STATES reported CREST PRO HEALTH problem on May 08, 2008. Female patient, weighting 140.0 lb, was diagnosed with dental disorder prophylaxis and was treated with CREST PRO HEALTH. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, tooth discolouration, . CREST PRO HEALTH dosage: unknown. Patient recovered.
Colgate Side Effects Report #5737918-3
COLGATE PRO HEALTH MOUTH RINSE problem was reported by a Consumer or non-health professional from UNITED STATES on May 12, 2008. Female patient, weighting 115.0 lb, was treated with COLGATE PRO HEALTH MOUTH RINSE. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, tooth discolouration, . COLGATE PRO HEALTH MOUTH RINSE dosage: unknown. Patient recovered.
Zetia Side Effects Report #5709440-1
Consumer or non-health professional from UNITED STATES reported ZETIA problem on Apr 17, 2008. Female patient, 73 years of age, weighting 115.0 lb, was diagnosed with blood cholesterol increased and was treated with ZETIA. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, lip dry, mouth ulceration, polydipsia, . ZETIA dosage: 30 MG 1 1 X DAY. Patient died.