Please choose an event type to view the corresponding MedsFacts report:

ABDOMINAL PAIN ( 7 FDA reports)
URETERIC OBSTRUCTION ( 7 FDA reports)
RENAL PAPILLARY NECROSIS ( 7 FDA reports)
HYDRONEPHROSIS ( 7 FDA reports)
ANURIA ( 7 FDA reports)
BLOOD UREA INCREASED ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 7 FDA reports)
INTENTIONAL OVERDOSE ( 6 FDA reports)
HYPOTENSION ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
SEROTONIN SYNDROME ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
DISORIENTATION ( 5 FDA reports)
RETCHING ( 5 FDA reports)
AGITATION ( 5 FDA reports)
PERSONALITY DISORDER ( 5 FDA reports)
PERIPHERAL COLDNESS ( 5 FDA reports)
GRAND MAL CONVULSION ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
MALAISE ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ( 4 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
ALCOHOL USE ( 3 FDA reports)
VOMITING ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
PUSTULAR PSORIASIS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
HYPERPROTEINAEMIA ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CALCIUM IONISED INCREASED ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)

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