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

DIARRHOEA ( 10 FDA reports)
NAUSEA ( 9 FDA reports)
VOMITING ( 9 FDA reports)
PRURITUS ( 8 FDA reports)
RASH ( 6 FDA reports)
FATIGUE ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
PAIN ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HEPATITIS CHOLESTATIC ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PLEURAL FIBROSIS ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PULMONARY TUBERCULOSIS ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FALL ( 1 FDA reports)
FEAR ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE NECROSIS ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INFUSION SITE ULCER ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THIRST ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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