DEVICE FAILURE side effect
What is DEVICE FAILURE ?Drugs associated with DEVICE FAILURE
ACYCLOVIR ADVAIR ALBUTEROL ALDURAZYME AMIDATE ANIMAS ASMANEX AVONEX BECLOMETASONE BETASERON BYETTA CAVERJECT CEREZYM CEREZYME CERVICAL CLARAVIS CLIMARA DAYTRANA DIASTAT DIAZEPAM DILANTIN DOBUTAMINE DOPAMINE DURAGESIC ENBREL EPINEPHERINE EPINEPHRINE FENTANYL FLOLAN FLUTICASONE FORASEQ FORTEO GLUCAGEN GLUCOSE HEPARIN HUMALOG HUMIRA IMITREX INOMAX INTRALIPID LEVEMIR LIORESAL MIACALCIN MORPHINE MYOZYME NATALIZUMAB NEUPRO NOVOLOG NOVORAPID OPTICLIKECTION PHENYTOIN PRIALT PRIMATENE PROAIR PROVENTIL REBIF SUPRANE SYMBICORT TAXUS TODAY TWINJECT TYSABRI VIAGRA XALATAN ZOLOFTDEVICE FAILURE : Humalog Side Effects Report #5669246-9
Consumer or non-health professional from UNITED STATES reported HUMALOG problem on Mar 13, 2008. Male patient, 69 years of age, weighting 170.0 lb, was diagnosed with diabetes mellitus and was treated with HUMALOG. After drug was administered, patient experienced the following problems/side effects: device failure, . HUMALOG dosage: unknown. Patient recovered.
DEVICE FAILURE : Symbicort Side Effects Report #5673044-X
SYMBICORT problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 14, 2008. Female patient, 55 years of age, weighting 210.1 lb, was diagnosed with asthma and was treated with SYMBICORT. After drug was administered, patient experienced the following problems/side effects: device failure, odynophagia, sensation of foreign body, . SYMBICORT dosage: unknown. Patient recovered.
DEVICE FAILURE : Duragesic Side Effects Report #5673209-7
Physician from UNITED STATES reported DURAGESIC problem on Mar 12, 2008. Male patient, weighting 170.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device failure, . DURAGESIC dosage: unknown. During the same period patient was treated with NEURONTIN, ZOLOFT, CEPHALEXIN, CIPROFLOXACIN, WARFARIN, FUROSEMIDE. Patient died on 11/11/2004.
DEVICE FAILURE : Proventil Side Effects Report #5678109-4
PROVENTIL problem was reported by a Health Professional from UNITED STATES on Mar 24, 2008. Female patient, 41 years of age, weighting 179.0 lb, was diagnosed with asthma and was treated with PROVENTIL. After drug was administered, patient experienced the following problems/side effects: device failure, . PROVENTIL dosage: unknown. Patient recovered.
DEVICE FAILURE : Twinject Side Effects Report #5679855-9
Consumer or non-health professional from CANADA reported TWINJECT problem on Mar 11, 2008. Male patient, 46 years of age, was diagnosed with anaphylactic reaction and was treated with TWINJECT. After drug was administered, patient experienced the following problems/side effects: device failure, . TWINJECT dosage: 0.3 MG, SUBCUTANEOUS/INTRAMUSCULAR. During the same period patient was treated with ZADITEN, NEXIUM, CETIRIZINE, NASONEX, INHALER, PREDNISONE. Patient recovered.
DEVICE FAILURE : Proair Side Effects Report #5682738-1
PROAIR HFA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 26, 2008. Female patient, 38 years of age, weighting 190.0 lb, was diagnosed with asthma and was treated with PROAIR HFA. After drug was administered, patient experienced the following problems/side effects: device failure, . PROAIR HFA dosage: unknown. Patient recovered.
DEVICE FAILURE : Fentanyl Side Effects Report #5683878-3
Pharmacist from UNITED STATES reported FENTANYL problem on Mar 27, 2008. Male patient, weighting 185.0 lb, was treated with FENTANYL. After drug was administered, patient experienced the following problems/side effects: device failure, . FENTANYL dosage: unknown. Patient recovered.
DEVICE FAILURE : Proair Side Effects Report #5688334-4
PROAIR HFA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 28, 2008. Male patient, 29 years of age, weighting 195.0 lb, was diagnosed with asthma and was treated with PROAIR HFA. After drug was administered, patient experienced the following problems/side effects: device failure, . PROAIR HFA dosage: unknown. Patient recovered.
DEVICE FAILURE : Byetta Side Effects Report #5688340-X
Pharmacist from UNITED STATES reported BYETTA problem on Mar 28, 2008. Female patient, 40 years of age, was diagnosed with diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: device failure, injection site discomfort, injection site haemorrhage, . BYETTA dosage: unknown. Patient recovered.
DEVICE FAILURE : Duragesic Side Effects Report #5610544-2
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 25, 2008. Female patient, weighting 194.0 lb, was diagnosed with migraine, pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device failure, . DURAGESIC dosage: unknown. During the same period patient was treated with DIPHENHYDRAMINE, LORAZEPAM, ALPRAZOLAM, PAROXETINE, VALIUM. Patient died on 03/01/2005.
DEVICE FAILURE : Novorapid Side Effects Report #5615657-7
Physician from JAPAN reported NOVORAPID CHU FLEXPEN problem on Jan 28, 2008. Female patient, weighting 119.0 lb, was diagnosed with type 1 diabetes mellitus and was treated with NOVORAPID CHU FLEXPEN. After drug was administered, patient experienced the following problems/side effects: device failure, gastroenteritis, hyperglycaemia, . NOVORAPID CHU FLEXPEN dosage: unknown. During the same period patient was treated with LANTUS. Patient was hospitalized. Patient recovered.
DEVICE FAILURE : Epinephrine Side Effects Report #5616305-2
EPINEPHRINE problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 22, 2008. Male patient, child 10 years of age, was diagnosed with anaphylactic reaction and was treated with EPINEPHRINE. After drug was administered, patient experienced the following problems/side effects: device failure, medical device complication, . EPINEPHRINE dosage: 0.3 MG INTRAMUSCULAR. Patient recovered.
DEVICE FAILURE : Duragesic Side Effects Report #5621277-0
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Jan 30, 2008. Male patient, weighting 240.0 lb, was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device failure, overdose, . DURAGESIC dosage: unknown. Patient died on 01/30/2004.
DEVICE FAILURE : Lioresal Side Effects Report #5625454-4
LIORESAL problem was reported by a Physician from UNITED STATES on Jan 30, 2008. Male patient, 17 years of age, was diagnosed with muscle spasticity and was treated with LIORESAL. After drug was administered, patient experienced the following problems/side effects: device failure, hypertonia, mental status changes, pruritus, . LIORESAL dosage: unknown. Patient was hospitalized. Patient recovered.
DEVICE FAILURE : Lioresal Side Effects Report #5628901-7
Physician from UNITED STATES reported LIORESAL problem on Feb 04, 2008. Male patient was diagnosed with muscle spasticity and was treated with LIORESAL. After drug was administered, patient experienced the following problems/side effects: device failure, muscle spasticity, paraesthesia, pneumonia, . LIORESAL dosage: unknown. Patient was hospitalized. Patient recovered.
DEVICE FAILURE : Novolog Side Effects Report #5629432-0
NOVOLOG problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 08, 2008. Female patient was diagnosed with insulin-requiring type 2 diabetes mellitus and was treated with NOVOLOG. After drug was administered, patient experienced the following problems/side effects: device failure, injection site infection, . NOVOLOG dosage: unknown. During the same period patient was treated with GLYBURIDE. Patient was hospitalized. Patient recovered.
DEVICE FAILURE : Epinephrine Side Effects Report #5631529-6
Consumer or non-health professional from UNITED STATES reported EPINEPHRINE problem on Jan 30, 2008. Female patient, weighting 150.0 lb, was diagnosed with hypersensitivity and was treated with EPINEPHRINE. After drug was administered, patient experienced the following problems/side effects: device failure, . EPINEPHRINE dosage: 0.3 MG INTRAMUSCULAR. During the same period patient was treated with XOPENEX, GUAIFENESIN, ALLEGRA, PREVACID, FLAXSEED OIL, SENNA, ASCORBIC ACID. Patient recovered.
DEVICE FAILURE : Levemir Side Effects Report #5632896-X
LEVEMIR problem was reported by a Consumer or non-health professional from BRAZIL on Feb 13, 2008. Female patient was treated with LEVEMIR. After drug was administered, patient experienced the following problems/side effects: device failure, hyperglycaemia, thyroid cancer, . LEVEMIR dosage: unknown. Patient was hospitalized. Patient recovered.
DEVICE FAILURE : Duragesic Side Effects Report #5634390-9
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Feb 13, 2008. Male patient, weighting 240.0 lb, was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device failure, overdose, . DURAGESIC dosage: unknown. Patient died on 01/30/2004.
DEVICE FAILURE : Duragesic Side Effects Report #5636836-9
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 13, 2008. Female patient, weighting 180.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device failure, . DURAGESIC dosage: unknown. During the same period patient was treated with VANCOMYCIN, AMITRIPTYLINE, LOVENOX, XANAX, NIZORAL. Patient died on 08/24/2004.
DEVICE FAILURE : Humira Side Effects Report #5636924-7
Consumer or non-health professional from CANADA reported HUMIRA problem on Feb 15, 2008. Female patient, weighting 154.1 lb, was diagnosed with psoriatic arthropathy, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: device failure, musculoskeletal pain, . HUMIRA dosage: unknown. During the same period patient was treated with LANSOPRAZOLE, FOLIC ACID, TELMISARTAN, ZOPICLONE, AMITRIPTYLINE HYDROCHLORIDE, METHOTREXATE. Patient was hospitalized. Patient recovered.
DEVICE FAILURE : Primatene Side Effects Report #5639712-0
PRIMATENE MIST problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 29, 2008. Male patient was diagnosed with asthma and was treated with PRIMATENE MIST. After drug was administered, patient experienced the following problems/side effects: device failure, . PRIMATENE MIST dosage: unknown. Patient recovered.
DEVICE FAILURE : Opticlikection Side Effects Report #5581573-2
Consumer or non-health professional from UNITED STATES reported OPTICLIKECTION INSULINDEVICE SANOFI AVENTIS problem on Jan 02, 2008. Female patient, 59 years of age, weighting 107.0 lb, was treated with OPTICLIKECTION INSULINDEVICE SANOFI AVENTIS. After drug was administered, patient experienced the following problems/side effects: device failure, . OPTICLIKECTION INSULINDEVICE SANOFI AVENTIS dosage: unknown. Patient recovered.
DEVICE FAILURE : Fentanyl Side Effects Report #5581921-3
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 25, 2007. Male patient, weighting 161.0 lb, was diagnosed with back pain and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: device failure, narcotic intoxication, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, CARISOPRODOL, CELEBREX, EFFEXOR, ESTRATEST H, GABAPENTIN, OXYCONTIN, WARFARIN. Patient died on 03/02/2005.
DEVICE FAILURE : Epinephrine Side Effects Report #5584208-8
Physician from UNITED STATES reported EPINEPHRINE problem on Dec 18, 2007. Male patient was diagnosed with anaphylactic reaction and was treated with EPINEPHRINE. After drug was administered, patient experienced the following problems/side effects: device failure, . EPINEPHRINE dosage: 0.3 MG, INTRAMUSCULAR. During the same period patient was treated with ALBUTEROL, ALLEGRA, ASMANEX TWISTHALER, SINGULAIR, XOLAIR. Patient recovered.
DEVICE FAILURE : Acyclovir Side Effects Report #5590355-7
ACYCLOVIR problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 09, 2008. Male patient was diagnosed with viral infection and was treated with ACYCLOVIR. After drug was administered, patient experienced the following problems/side effects: device failure, . ACYCLOVIR dosage: unknown. Patient recovered.
DEVICE FAILURE : Today Side Effects Report #5591240-7
Health Professional from UNITED STATES reported TODAY SPONGE SYNOVA HEALTHCARE problem on Jan 10, 2008. Female patient, 38 years of age, weighting 160.0 lb, was diagnosed with contraception and was treated with TODAY SPONGE SYNOVA HEALTHCARE. After drug was administered, patient experienced the following problems/side effects: device failure, pregnancy with contraceptive device, . TODAY SPONGE SYNOVA HEALTHCARE dosage: unknown. Patient recovered.
DEVICE FAILURE : Epinephrine Side Effects Report #5593271-X
EPINEPHRINE problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 28, 2007. Female patient, weighting 113.0 lb, was diagnosed with anaphylactic reaction and was treated with EPINEPHRINE. After drug was administered, patient experienced the following problems/side effects: device failure, heart rate increased, tremor, . EPINEPHRINE dosage: (0.3 MG, SUBCUTANEOUS). During the same period patient was treated with XOPENEX, ADVAIR DISKUS, ATROVENT, ASTELIN, TOPIRAMATE, RELPAX. Patient recovered.
DEVICE FAILURE : Novorapid Side Effects Report #5599960-5
Physician from JAPAN reported NOVORAPID CHU FLEXPEN problem on Jan 15, 2008. Female patient, weighting 119.0 lb, was diagnosed with type 1 diabetes mellitus and was treated with NOVORAPID CHU FLEXPEN. After drug was administered, patient experienced the following problems/side effects: device failure, gastroenteritis, hyperglycaemia, . NOVORAPID CHU FLEXPEN dosage: unknown. During the same period patient was treated with LANTUS. Patient was hospitalized. Patient recovered.
DEVICE FAILURE : Humira Side Effects Report #5606766-7
HUMIRA problem was reported by a Consumer or non-health professional from CANADA on Jan 19, 2008. Female patient, weighting 154.1 lb, was diagnosed with psoriatic arthropathy, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: device failure, musculoskeletal pain, . HUMIRA dosage: unknown. During the same period patient was treated with LANSOPRAZOLE, FOLIC ACID, TELMISARTAN, ZOPICLONE, AMITRIPTYLINE HYDROCHLORIDE, METHOTREXATE. Patient was hospitalized. Patient recovered.
DEVICE FAILURE : Proair Side Effects Report #5608733-6
Consumer or non-health professional from UNITED STATES reported PROAIR HFA problem on Jan 28, 2008. Female patient, 43 years of age, weighting 140.0 lb, was diagnosed with asthma and was treated with PROAIR HFA. After drug was administered, patient experienced the following problems/side effects: device failure, . PROAIR HFA dosage: unknown. Patient recovered.
DEVICE FAILURE : Primatene Side Effects Report #5614009-3
PRIMATENE MIST problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 08, 2008. Female patient was diagnosed with asthma and was treated with PRIMATENE MIST. After drug was administered, patient experienced the following problems/side effects: device failure, . PRIMATENE MIST dosage: unknown. Patient recovered.
DEVICE FAILURE : Enbrel Side Effects Report #5543918-9
Physician from UNITED STATES reported ENBREL problem on Dec 05, 2006. Female patient was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: device failure, foot operation, intervertebral disc protrusion, . ENBREL dosage: unknown. Patient recovered.
DEVICE FAILURE : Duragesic Side Effects Report #5562574-7
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 06, 2007. Female patient, weighting 125.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device failure, . DURAGESIC dosage: unknown. During the same period patient was treated with VALIUM, BUPROPION, VALPROIC ACID, OLANZAPINE. Patient died on 09/11/2004.
DEVICE FAILURE : Glucagen Side Effects Report #5562784-9
Physician from FRANCE reported GLUCAGEN problem on Dec 06, 2007. Male patient, 64 years of age, was treated with GLUCAGEN. After drug was administered, patient experienced the following problems/side effects: device failure, injection site vesicles, . GLUCAGEN dosage: unknown. During the same period patient was treated with NOVORAPID, LANTUS. Patient was hospitalized. Patient recovered.
DEVICE FAILURE : Proventil Side Effects Report #5564810-X
PROVENTIL problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 14, 2007. Female patient, weighting 170.0 lb, was treated with PROVENTIL. After drug was administered, patient experienced the following problems/side effects: device failure, . PROVENTIL dosage: unknown. Patient recovered.
DEVICE FAILURE : Dilantin Side Effects Report #5567515-4
Consumer or non-health professional from UNITED STATES reported DILANTIN problem on Dec 11, 2007. Female patient was treated with DILANTIN. After drug was administered, patient experienced the following problems/side effects: device failure, gingival bleeding, gingival hyperplasia, gingival swelling, . DILANTIN dosage: unknown. Patient recovered.
DEVICE FAILURE : Albuterol Side Effects Report #5570367-X
ALBUTEROL SULPHATE problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 19, 2007. Male patient, 53 years of age, weighting 150.0 lb, was diagnosed with asthma and was treated with ALBUTEROL SULPHATE. After drug was administered, patient experienced the following problems/side effects: device failure, . ALBUTEROL SULPHATE dosage: unknown. Patient recovered.
DEVICE FAILURE : Duragesic Side Effects Report #5571870-9
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Dec 10, 2007. Female patient, weighting 194.0 lb, was diagnosed with migraine, pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device failure, . DURAGESIC dosage: unknown. During the same period patient was treated with DIPHENHYDRAMINE. Patient died on 03/01/2005.
DEVICE FAILURE : Humalog Side Effects Report #5572911-5
HUMALOG problem was reported by a Pharmacist from UNITED STATES on Dec 19, 2007. Female patient was treated with HUMALOG. After drug was administered, patient experienced the following problems/side effects: device failure, . HUMALOG dosage: unknown. Patient recovered.
DEVICE FAILURE : Lioresal Side Effects Report #5573946-9
Physician from UNITED STATES reported LIORESAL problem on Dec 10, 2007. Male patient was diagnosed with muscle spasticity and was treated with LIORESAL. After drug was administered, patient experienced the following problems/side effects: device failure, incorrect dose administered, overdose, unresponsive to stimuli, . LIORESAL dosage: unknown. Patient was hospitalized. Patient recovered.
DEVICE FAILURE : Epinephrine Side Effects Report #5578139-7
EPINEPHRINE problem was reported by a Consumer or non-health professional from CANADA on Dec 11, 2007. Female patient was diagnosed with anaphylactic reaction and was treated with EPINEPHRINE. After drug was administered, patient experienced the following problems/side effects: device failure, dyspnoea, obstructive airways disorder, . EPINEPHRINE dosage: (0.3 MG INTRAMUSCULAR). Patient was hospitalized. Patient recovered.
DEVICE FAILURE : Lioresal Side Effects Report #5578877-6
Physician from UNITED STATES reported LIORESAL problem on Dec 20, 2007. Female patient was diagnosed with muscle spasticity and was treated with LIORESAL. After drug was administered, patient experienced the following problems/side effects: device failure, rash, . LIORESAL dosage: unknown. Patient recovered.
DEVICE FAILURE : Foraseq Side Effects Report #5504030-8
FORASEQ problem was reported by a Consumer or non-health professional from BRAZIL on Oct 29, 2007. Female patient was treated with FORASEQ. After drug was administered, patient experienced the following problems/side effects: device failure, diabetes mellitus, hyperhidrosis, insomnia, irritability, mydriasis, nervousness, visual disturbance, . FORASEQ dosage: unknown. Patient recovered.
DEVICE FAILURE : Animas Side Effects Report #5508881-5
Consumer or non-health professional from UNITED STATES reported ANIMAS problem on Nov 05, 2007. Female patient, weighting 30.00 lb, was treated with ANIMAS. After drug was administered, patient experienced the following problems/side effects: device failure, medical device complication, . ANIMAS dosage: unknown. Patient recovered.
DEVICE FAILURE : Proair Side Effects Report #5513716-0
PROAIR HFA problem was reported by a Pharmacist from UNITED STATES on Nov 09, 2007. Male patient, 48 years of age, was treated with PROAIR HFA. After drug was administered, patient experienced the following problems/side effects: device failure, . PROAIR HFA dosage: unknown. Patient recovered.
DEVICE FAILURE : Duragesic Side Effects Report #5514100-6
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Nov 05, 2007. Male patient, weighting 255.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device failure, narcotic intoxication, . DURAGESIC dosage: unknown. During the same period patient was treated with HYDROCODONE BITARTRATE AND ACETAMINOPHEN, LIDODERM, AMBIEN, VALIUM, ELAVIL. Patient died on 07/13/2004.
DEVICE FAILURE : Epinephrine Side Effects Report #5517713-0
EPINEPHRINE problem was reported by a Health Professional from UNITED STATES on Oct 25, 2007. Female patient, weighting 240.0 lb, was diagnosed with anaphylactic reaction and was treated with EPINEPHRINE. After drug was administered, patient experienced the following problems/side effects: device failure, . EPINEPHRINE dosage: unknown. Patient recovered.
DEVICE FAILURE : Duragesic Side Effects Report #5519083-0
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Nov 05, 2007. Female patient, weighting 180.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device failure, therapeutic agent toxicity, . DURAGESIC dosage: unknown. During the same period patient was treated with VANCOMYCIN, AMITRIPTYLINE, LOVENOX, XANAX, NIZORAL. Patient died on 08/24/2004.
DEVICE FAILURE : Enbrel Side Effects Report #5519242-7
ENBREL problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 07, 2007. Female patient was diagnosed with rheumatoid arthritis, juvenile arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: device failure, hypoaesthesia, joint range of motion decreased, rheumatoid arthritis, spondylitis, . ENBREL dosage: unknown. During the same period patient was treated with METHOTREXATE. Patient was hospitalized. Patient recovered.
DEVICE FAILURE : Enbrel Side Effects Report #5519263-4
Consumer or non-health professional from UNITED STATES reported ENBREL problem on Nov 06, 2007. Male patient was diagnosed with psoriatic arthropathy, psoriasis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: device failure, psoriasis, rotator cuff syndrome, spinal fusion surgery, . ENBREL dosage: unknown. Patient was hospitalized. Patient recovered.