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

FATIGUE ( 20 FDA reports)
DIARRHOEA ( 14 FDA reports)
HEADACHE ( 14 FDA reports)
MALAISE ( 14 FDA reports)
ANGER ( 12 FDA reports)
BLOOD PRESSURE INCREASED ( 12 FDA reports)
CONFUSIONAL STATE ( 12 FDA reports)
EYELID DISORDER ( 12 FDA reports)
FLUSHING ( 12 FDA reports)
NASAL CONGESTION ( 12 FDA reports)
NAUSEA ( 12 FDA reports)
SPEECH DISORDER ( 12 FDA reports)
STRESS ( 12 FDA reports)
SWELLING ( 12 FDA reports)
PAIN IN EXTREMITY ( 11 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 10 FDA reports)
SLUGGISHNESS ( 10 FDA reports)
OEDEMA PERIPHERAL ( 9 FDA reports)
RASH ( 9 FDA reports)
SWELLING FACE ( 9 FDA reports)
CHEST PAIN ( 8 FDA reports)
RESPIRATORY RATE INCREASED ( 7 FDA reports)
TACHYCARDIA ( 7 FDA reports)
COUGH ( 6 FDA reports)
DYSPHONIA ( 6 FDA reports)
DYSPNOEA EXERTIONAL ( 6 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 6 FDA reports)
INFLUENZA ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
SPUTUM DISCOLOURED ( 6 FDA reports)
ANXIETY ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
MOUTH ULCERATION ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 4 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHILLS ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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